Neudle.com: reflexes absent

Differential
(Click to cross reference)

abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abducens nerve paralysis, children

acanthocytosis

accomodation, abnormal

acoustic nerve

acquired immunodeficiency syndrome

acral sensory symptoms

ACTH, ectopic syndrome of

acute ataxia of childhood

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

Addison's disease

Adies pupil

adverse drug reaction

aggression

alcohol

alcohol intolerance

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

alkylating agents

alopecia

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

aminoacidurias

amphiphysin antibodies

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis-like syndrome

ANA

anal wink response

ANA-negative systemic lupus erythematosus

anemia

anesthesia, general

aneurysm, intracranial

anterior horn cell disease

anterior spinal artery

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti GQ1b IgG antibody

anti MAG antibodies

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticoagulant, treatment

antidepressant

antiganglioside antibodies

apraxia of eye movements

ataxia telangiectasia

auditory evoked brainstem potentials

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

bedridden

behavioral disorder

Bell's phenomenon

benign essential tremor

beriberi

bicaudate index

Bickerstaff's brainstem encephalitis

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow suppression

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

Brown-Vialetto-Van Laere syndrome

burst suppression pattern, electroencephalogram

cachexia

calf hypertrophy

campylobacter infection

carcinoma of pancreas

carcinoma of stomach

cardiac arrest

cardiac arrest and resuscitation

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, emission, abnormal

catalepsy

cataracts

cauda equina

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous sinus

cavernous sinus syndrome, bilateral

cavernous sinus, syndrome

CD4 counts

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral edema

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

children

chills

Chinese paralytic syndrome

choreoathetosis, paroxysmal

choroid plexus

chromosomal abnormality

chronic graft versus host disease

chronic idiopathic anhidrosis

cimetidine

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

congenital heart disease

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

conus medullaris, lesion of

convergence, impaired

conversion reaction

cornea, abnormal

cornea, opacity of

corneal reflex, abnormal

corneal reflex, absent

coronavirus

corpus callosum, lesion of

cough

COVID-19

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cystic fibrosis, neurologic complications with

cystoisospora belli

cytokines

cytomegalovirus infection

deafness

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia, transmissible

denervation of muscle

denervation potentials

depression

dermatitis

descending paralysis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, chemical

diagnosis

diagnostic criteria

dialysis

diaphragmatic paralysis

diarrhea

dideoxycytidine

dieting

differential diagnosis

difficulty climbing stairs

dilantin

diplegia, brachial

diplopia

dislocated hip, congenital

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diuretic

dizziness

dopa responsive dystonia

down-beat nystagmus

drowsiness

drug induced neurologic disorders

drug induced neurologic disorders in children

dyskinesia, buccal lingual facial

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

electrophoretic pattern, serum

ELISA

emergencies, neurologic

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, anoxic

encephalopathy, progressive

enteritis

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

episodic disorders

episodic neurologic deficits

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

eye closure

eye movement, disorders of

face, elongated

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial sweating, unilateral

facial weakness

facial weakness, bilateral

failed medical management

fine motor function, impaired

fingernails, abnormal

Fisher C.M.

Fisher's syndrome

Fisher's syndrome, atypical

fluorescent treponema antibody absorption(FTA-ABS)

Friedreich's ataxia, late onset

fundus, abnormality of

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

general paresis of the insane

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioma

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

glutamic acid decarboxylase, antibody

gluten-free diet

Gowers maneuver

granuloma, eosinophilic

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, neuropathology of inflammatory lesion of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination

hallucination, auditory

heavy metal intoxication

heel-knee-shin test

hemidiaphragm, paralysis of

hemoglobinuria

hemorrhagic diathesis

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex virus

herpes virus

herpes virus infection

histamine-2 receptor blockers

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, communicating

hyperemisis gravidarum

hypokalemic alkalosis

hypokalemic paralysis

hypokalemic periodic paralysis

hyponatremia

hypoosmolality of serum

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophonia

hypophosphatemia

hypopigmentation of skin

hyporeflexia

hypotension, systemic

iatrogenic neurologic disorders

idiopathic

ileus, paralytic

imbalance

immune checkpoint inhibitors

immunoelectrophoresis, serum

immunofluorescence

immunofluorescent"band"test

immunosuppression

immunosuppressive agents

impotence

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incoordination

India

infant, evaluation of

infantile neuronal degeneration

infection

insecticides

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal obstruction

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

intraneural hemorrhage

intrathecal chemotherapy

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

leg weakness, bilateral

leg weakness, unilateral

lethargy

leukemia

leukemia, neurologic findings assoc.with

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life support, withdrawal of

light-near dissociation, causes of

liver function enzymes

long bone lesion

Lowe's syndrome

lumbosacral radiculopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macrocephaly

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malignancy, occult

malignant hyperpyrexia

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningitis, carcinomatous

meningitis, elderly

meningitis, leukemic

meningitis, lupus

meningitis, lymphomatous

meningitis, meningococcal

meningitis, neutrophilic

meningitis, prevention

meningitis, prophylaxis against

meningitis, recurrent

meningitis, syphilitic

meningoencephalitis

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic acidosis

methotrexate

methyl bromide

methylhydrazine derivatives

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

modafinil

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

mononeuropathy multiplex

mononeuropathy, children

movement disorder, drug induced

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gradient-echo

MRI, high signal foci on

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, sulcal hyperintensity

multicore myopathy

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple organ failure

multiple sclerosis

multiple sclerosis, acute

multiple sleep latency test

muscle atrophy, progressive

muscle atrophy, static

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, LAMA2

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, etiology of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myelogram

myelogram, cervical

myelogram, complications of

myelogram, metrizamide

myeloma, osteosclerotic

myelomalacia

myelopathy

myelopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, drug-induced

myopathy, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, steroid induced

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve growth factor

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuritis, heavy metals causing

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic examination, abnormal

neurologic signs

neurologic symptoms

neurological intensive care

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia

neuron specific enolase

neuronal intranuclear inclusion disease

neuronal loss

neuronopathy

neuronopathy, sensory

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, asymptomatic

neuropathy, ataxic

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

next-generation sequencing

nonsteroidal anti-inflammatory drug

NOTCH2NLC

numbness, ascending

numbness, extremity

numbness, generalized

nusinersen

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, vertical

obesity

occupational neurologic disorders

oculocephalic reflex

oculovestibular reflex

old age, neurology of

one and a half syndrome

opened mouth

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, neonatal

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic nerve

optic nerve, enhancement

optic nerve, hypoplasia of

optic neuritis

optic neuritis, bilateral

optic neuropathy

oral contraceptives

organ transplantation

organomegaly

oropharyngeal weakness

orthopnea

orthostatic hypotension

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic ganglionopathy

parenteral alimentation

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pericardial friction rub

pericarditis

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

photosensitivity, skin

plasma cell dyscrasia

plasmacytoma

plasmapheresis

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poliomyelitis-like illness

polycystic kidneys

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuritis

polyneuritis, acute sensory

polyneuropathy

polyneuropathy, acute sensory

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyneuropathy, familial

polyneuropathy, lymphomatous

polyneuropathy, subacute idiopathic demyelinating

polyneuropathy, uremic

polyradiculoneuropathy

position sensation, abnormal

positional head-hanging test

positive sharp waves

posterior column disease

postinfectious

postoperative neurologic complications

potassium

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

prevention of neurologic disorders

prion disease

procarbazine

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

prolactin, elevated

proprioception

proprioception, abnormal

pseudointernuclear ophthalmoplegia

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pulmonary nodules

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, unilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriparesis

quadriparesis, progressive

quadriplegia

quadriplegia, transient

rabies, nervous system involvement with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

real-time quaking-induced conversion

recurrent

reflex, brainstem

reflex, brainstem, absent

reflex, cutaneous

REM sleep

remote effect of cancer on the nervous system

renal failure

renal failure, acute

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

reticular activating system

reticulum cell sarcoma

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

riboflavin

riboflavin transporter deficiency

saccadic eye movements, abnormal

scoliosis, neurologic association with

sedimentation rate, elevated

segmental demyelination

seizure

seizure, children

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, patchy

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

septicemia

serologic testing

serum alanine aminotransferase

serum lipase, elevated

severe acute respiratory syndrome

short stature

shunt procedure, ventricular

Shy-Drager syndrome

simvastatin

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

slurred speech

small vessel vasculitis

speech disorder, childhood

speech disorder, non aphasic

spinal cord

spinal cord, enlargement

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

spironolactone

splenomegaly

spongy degeneration of brain

spontaneous remission

stem cell transplantation

steppage gait

steroid

steroid therapy, CNS treatment and complications with

superior oblique palsy

suspended sensory loss

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

tensilon test, false positive

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thyroid function tests

tick-borne encephalitis

tinnitus

titinopathy

toe walking

tomaculous neuropathy

tongue, biting

tongue, fasciculations of

tongue, impaired movements of

tongue, numbness of

tongue, weakness

tonic spasms

tonsillar herniation of cerebellum

toxic encephalopathy

toxins, nervous system

transient neurologic deficit

transverse smile

trauma

travel, foreign

treatment of neurologic disorder

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

ulcerative colitis

ulnar neuropathy

ultrasonography, nerve

urine osmolality, elevated

urine test for metabolic disorders

urine test in toxic screen

urine, dark

vaccination, neurologic complications with

vascular endothelial growth factor

vasculitides

vectors of infection

vecuronium

Venereal Disease Research Laboratory test

vertigo

vestibulopathy

vibratory sensation

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

visual acuity, decreased

visual evoked response

vitamin supplementation

vocal cord paralysis

vocalizations

voice, abnormality of

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

Watson-Schwartz reaction

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weakness, severe

weaning from respirator, failure to

weight gain

weight loss

Wernicke's encephalopathy

X-linked bulbospinal neuronopathy

x-linked mental retardation

Showing articles 200 to 250 of 573 << Previous Next >>

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Recurrent Aseptic Meningitis in an Elderly Male, Unusual Prodromal Manifestation of SLE
JAMA 235:1142, Finelli,P.F.,et al, 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Acute Areflexic Paralysis
Arch Neurol 32:706, Furlan,A.J.,et al, 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
Am J Ophthalmol 77:725, Swick,H.M., 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Lumbosacral Radiculomyelitis Assoc with Pandemic Acute Hemorrhagic Conjunctivitis
Letter Lancet Feb 1973., Wadia,N.H.,et al, 1973

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

Acute Intermittent Porphyria
Medicine 49:1, Stein,J.,et al, 1970

Ocular Complications of Vincristine Therapy
Arch Ophthalmol 78:709, Albert,D.M.,et al, 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Addison's Disease, In The Diagnosis of Stupor & Coma
& Posner, J. , FA Davis Co. 1966, p. 145-146., Plum,F., 1966

Neuro CPC of MGH
Multiple Sclerosis, Cerebral Infarcts, & Colitis, NEJM 268:607-615., , 1963

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Postural Tachycardia Syndrome
www.UptoDate.com,Aug, Cheshire,W.P., 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

An Unusual Case of Acute Psychosis and Tetraparesis in a Young Zambian Man
Neurol 97:1002-1005, Zimba, S.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,et al, 2020

Neurologic Features in Severe SARS-CoV-2 Infection
NEJM 382:2268-2270, e110, , 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

A Middle Aged Man with Back Pain and Heavy Legs
BMJ 366:e2420, Chanchlani, N. & Reading, N.G., 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A 30-year-old man with acute paraplegia and left foot gangrene
Neurol 90:e1355-e1359, Paliwal, V.K.,et al, 2018

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