Neudle.com: X linked myopathy

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Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

allergic angiitis

amaurosis fugax

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anesthesia, general

angiotensin-converting enzyme

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

anti-myeloperoxidase

antineutrophil cytoplasmic autoantibodies

aortic valve, insufficiency

arcuate scotoma, differential diagnosis of

arrhythmia, cardiac

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

atrial fibrillation

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

bacterial infection

Balint's syndrome

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

bitemporal visual field defect

bone marrow suppression

bone marrow transplantation

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, tuberculoma of

burning paresthesia

calcification, intracranial

calcification, muscle

calf hypertrophy

carcinoma of lung

carcinoma of pancreas

cardiovascular disease

carpo-pedal spasm

CAT scan, abnormal

CAT scan, chest

CAT scan, muscle

cauda equina, lesion of

central nervous system, infection of

central nuclei, muscle

cerebellum, disease of

cerebellum, neoplasms of

cerebral infarction

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cervical spine abnormality

chest x-ray, abnormal

chromosomal abnormality

Churg-Strauss syndrome

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

Cogan's syndrome

collagen vascular disease

congenital myopathy

congestive heart failure

conjunctival injection

contractures, joint

corpus callosum, lesion of

corpus callosum, thinning

cranial nerve palsies

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

deafness, bilateral

deafness, unilateral

degenerative diseases of CNS

dementia, childhood

demyelinating disease

dermatomyositis

dermatomyositis, childhood

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin, hypersensitivity to

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dystonia, etiology of

dystonia, painful

dystrophic calcification

echocardiogram, transesophageal

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electronystagmography

electroretinograph

Emery-Dreifuss muscular dystrophy

encephalomyelitis

endocarditis, acute bacterial

endophthlamitis

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

erectile dysfunction

erythema multiforme

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

false positive VDRL

fatty acid, elevated plasma content

ferritin, elevated

fingernails, abnormal

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

fundus, abnormality of

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal bleeding

gaze palsy, horizontal

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gowers maneuver

granuloma, eosinophilic

granulomatosis, allergic

granulomatous disease

granulomatous hypophysitis

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

headache, bifrontal

headache, positional

heavy metal intoxication

heliotrope rash

hemangioblastoma

hematuria, microscopic

hemianopia, homonymous

hepatosplenomegaly

histochemistry of muscle

hormone replacement

Huntington's chorea

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperadrenalism

hyperamylasemia

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperinsulinism

hyperparathyroidism

hypersensitivity reaction

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypokalemic periodic paralysis

hypokinetic left ventricle

hypoparathyroidism

hypothalamus, disturbance of

iatrogenic neurologic disorders

immunohistochemistry

immunosuppressive agents

inclusion body myositis

intellectual deficit

interferonopathy

intestinal biopsy

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

islet cell tumor

Kawasaki disease

Kearns-Sayre syndrome

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

level of consciousness, decreased

life expectancy

livedo reticularis

liver function enzymes

lymphadenopathy

lymphadenopathy, hilar

lymphocyte capping, diminished

lymphoid adenohypophysitis

macular degeneration

malignant hyperpyrexia

mediastinum, mass of

medulla oblongata, lesion of

memory, impairment of

meningitis, aseptic

meningitis, basilar

meningitis, chronic

meningitis, recurrent

meningoencephalitis

meningomyelitis

mental retardation

mental retardation, familial

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

molecular genetics

mononeuritis multiplex

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

mucopolysaccharidoses

multiple sclerosis, misdiagnosis

muscle stiffness

muscle tenderness

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, receptor site in

myelitis, longitudinal

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myopathy, quadriceps

myopathy, vacuolar

myotonia dystrophica

myotonic discharges

myxedema, neurologic manifestations of

nasal septum, perforation of

nausea and vomiting

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

neuritis, heavy metals causing

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology, brain

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, toxic

neuropathy, vasculitic, systemic

night blindness

obsessive-compulsive disorder

ocular myopathy

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, total

optic neuropathy

orange peel appearance of skin

otitis, neurologic complications with

pain, abdominal

pain, testicular

paraparesis, spastic

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinsonism syndrome

periarteritis nodosa

pericardial effusion

periodic paralysis

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peroxisomal disease

pheochromocytoma

pigmentary retinopathy

pituitary, enlargement

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

polycystic kidneys

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis, eosinophilic

pons, lesion of

position sensation, abnormal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

prothrombin time, prolonged

proximal muscle atrophy

psychiatric problems in neurologic disorders

ptosis, bilateral

pulmonary edema

pulmonary infiltrates

pyloric stenosis

quadriceps atrophy

Raynaud's phenomenon

recombinant DNA

refractive errors

Refsum's disease

renal cell carcinoma

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal artery occlusion

retinal degeneration

retinal hemangioma

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rickettsial organism

rigid spine syndrome

rippling muscle disease

Rocky Mountain spotted fever

sarcoidosis, CNS

scleroderma, neurologic involvement with

sedimentation rate

sedimentation rate, elevated

seizure, familial

sella turcica, enlargement of

sensorineural hearing loss

serologic testing

serum alanine aminotransferase

severe acute respiratory syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

Southern immunoblot test

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinocerebellar degeneration

spirochete infection

splinter hemorrhages

standing difficulty

steroid therapy, CNS treatment and complications with

Stevens-Johnson syndrome

streptococcus pneumoniae

subarachnoid hemorrhage

subcutaneous edema

suprasellar lesion

sweating, abnormality of

systemic illness

systemic lupus erythematosus, drug induced

tandem gait, ataxic

tapetoretinal degeneration

telangiectases, periungual

testicular atrophy

testicular biopsy

testicular enlargement

third nerve palsy

thrombocytopenia

tongue, fasciculations of

tonsillar herniation of cerebellum

toxic encephalopathy

toxic oil syndrome

transient ischemic attack

travel, foreign

treatment of neurologic disorder

tremor, intention

tremor, postural

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

tuberculoma of CNS

tuberculosis, miliary

tumor necrosis factor inhibitor

uncal herniation

urine test in toxic screen

Usher's syndrome

Venereal Disease Research Laboratory test

very long chain fatty acids

vision, blurred

visual acuity, decreased, monocular

visual field defect

visual loss, sudden-unilateral

Von Hippel Lindau

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

Western immunoblot test

Whipple's disease

white matter disease

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

X-linked myopathy

x-linked myopathy with excessive autophagy

x-ray, cervical spine

Showing articles 50 to 100 of 1514 << Previous Next >>

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Preventive Screening for Fragile X Syndrome
Editorial, Lancet 2:1191-11921986., , 1986

Cogan's Syndrome:18 Cases & a Review of the Literature
Mayo Clin Proc 61:344-361, Vollertsen,R.S.,et al, 1986

Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Progressive Cervical Osteophytosis and Dysphagia Associated with Isotretinoin Treatment for Rosacea
Lancet 404:e4, Naraghi,K. & Marzo-Ortega,H., 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Lentiviral Gene Therapy for Cerebral adrenoleukodystrophy
NEJM 391:1302-1312,1358, Eichler,F.,et al, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Diagnosis and Management of ANCA-Associated Vasculitis
Lancet 403:683-698, Kronbichler, A., et al, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Hidden Metastatic Lung Tumour Diagnosed by AI
Lancet 403:1299, Muroya,D.,et al, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Neurologic Manifestations of Long COVID Differ Based on Acute COVID-19 Severity
Ann Neurol 94:146-159, Giraldo,G.S.P.,et al, 2023

Multiple "Rings" in the Brain
BMJ 383:e077299, Li,Y.et al, 2023

A 22-Year-Old Man with Multifocal Brain and Osseous Lesions
Neurol 101:1025-1031, Reddy,S.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Clinicopathologic Conference, Paraneoplastic Vasculitis of the Central Nervous System
NEJM 388:747-757, Case 6-2023, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Pathogenesis and Clinical Manifestations of IgG4-Related Disease
WWW.UptoDate.com, April, Moutsopoulos,H.M.,et al, 2023

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Babesiosis: Clinical Manifgestations and Diagnosis
www.UptoDate.com, Oct, Krause,P.J. & Vannier,E.G., 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

A Woman with Eosinophilic Brainstem Meningoencephalitis
JAMA Neurol 79:198-199, Fernandes Ferreira, L.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Showing articles 50 to 100 of 1514 << Previous Next >>