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Differential
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abulia

acanthosis nigricans

acquired immunodeficiency syndrome

acrochordon

acromegaly

acute intermittant porphyria

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenal crisis, acute

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

affect, inappropriate

agitation

Albright disease

alcohol

alcohol, neurologic complications with

anemia, megaloblastic

anterior horn cell disease

antibiotics

anticholinergic drugs

anticholinergic drugs, side effects of

aspartate aminotransferase

ataxia telangiectasia

autonomic dysfunction

azidodeoxythymidine

B 12 deficiency

B 12 deficiency, infants

Babinski sign

bacterial infection

bacterial infection, CNS

Bannayan-Riley-Ruvalcaba syndrome

basal ganglia, calcification of

basal ganglia, lesion of

bone marrow transplantation

bone pain

bone survey

bone survey, metastatic

brain atrophy

brain biopsy

brain natriuretic peptide

calcification, intracranial

calf hypertrophy

carbamazepine

carbon monoxide poisoning

cardiomyopathy

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery stenosis

carpal tunnel syndrome

Castleman's disease

CAT scan

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, disappearing lesion on

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cephalosporins

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral cortical atrophy

cerebral edema

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, red cells in

cerebrovascular accident

cervical spondylosis

chemotherapy, CNS treatment and complications with

children

chorionic gonadotropin

chromosome 19

cirrhosis

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

compartment syndrome, gluteal

complications

compression fracture

compression neuropathy

confusion

confusional state, acute

congenital malformation

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

cultured skin fibroblasts

demyelinating disease

depression

dermal sinus tract

dermatitis

dermatitis herpetiformis

dermatomyositis

dermoid

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

drug abuse, neonatal abstinence syndrome with

drug abuse, neurologic complications of

drug addiction

drug induced neurologic disorders

drug induced neurologic disorders in children

dystonia musculorum deformens

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electrophoretic pattern, serum

emergencies, neurologic

emotional lability

encephalomyopathy

encephalopathy

encephalopathy, metabolic

endarterectomy, carotid

endocarditis, infectious

endophthlamitis

enterovirus

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

epidermal nevus syndrome

epsilon-aminocaproic acid(E.A.C.A.)

etonogestrel

exercise

exercise intolerance

eye movement, disorders of

eye, pain in

face, numbness of

facial anomalies

facial appearance, abnormal

facial nerve

facial nerve palsy

facial pain

facial pain, atypical

fatty acid, elevated plasma content

fever

fibrillations

fibrous dysplasia

fibrous dysplasia of orbit

fine motor function, impaired

fingernails, abnormal

fingernails, white

fingers, abnormal

folic acid deficiency

follicle stimulating hormone

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glossitis

glossopharyngeal nerve

glossopharyngeal neuralgia

glucose tolerance test, abnormal

glycogen storage disease

hematuria, microscopic

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes simplex virus, human nervous system and

herpes simplex, neurocutaneous lesions in

hirsutism

histochemistry of muscle

HMGcoA reductase inhibitors

homocystinuria

hormone replacement

hormone therapy

human immunodeficiency virus type 1

hyperpigmentation of skin

hyponatremic encephalopathy

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hyporeflexia

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypothalamus, neoplasm of

hypothermia

hypothermia, causes of

hypothyroidism

hypotonia, infants

iatrogenic neurologic disorders

immunoelectrophoresis, serum

immunosuppressive agents

implant contraceptives

impotence

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion body myositis

incontinentia pigmenti

infant, evaluation of

infantile tremor syndrome

intellectual deterioration

intestinal biopsy

intracranial hypertension, benign

intracranial pressure, increased

intravenous drug abuse

irritability

ischemic exercise test

jaundice

jaw pain

lactic acidemia

lactic dehydrogenase(LDH)

learning disability

learning disability, in children

leg swelling

leg weakness, bilateral

leg weakness, unilateral

leukoencephalopathy, toxic

level of consciousness, decreased

liver function enzymes

liver transplantation

lymphoma involving CNS

macrocephaly

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malignant hyperpyrexia

McArdle's disease

McArdle's disease, adult onset

McCune-Albright syndrome

memory, impairment of

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methylmalonic acid, serum

mitochondrial disease

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

MRI, diffusion weighted

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

muscular dystrophy, limb-girdle

myeloma, osteosclerotic

myopathy, drug-induced

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myxedema, neurologic manifestations of

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neuroleptic

neuroleptic malignant syndrome

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuropathy, peripheral

neuropathy, peripheral, treatment

nutritional deficiency

nystagmus

ochronosis

oculomasticatory myorhythmia

ophthalmoplegia

optic atrophy

orange peel appearance of skin

PAS positive material in the brain

pellagra

penis, pigmented macules

periarteritis nodosa

periodic paralysis

peripheral blood smear, abnormal

phosphorylase b kinase deficiency

photic stimulation

photophobia

photosensitivity, skin

pigmentary retinopathy

pigmented macules

pituitary, adenoma

plasma cell dyscrasia

plasmacytoma

pleocytosis of cerebrospinal fluid

pleural effusion

pleurisy

POEMS syndrome

polycythemia, primary

polycythemia, secondary

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyps, gastrointestinal tract

porphyria

post herpetic neuralgia

posterior column disease

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognosis

progressive neurologic disorder

prolactin, elevated

proteinuria

proximal muscle atrophy

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, dilated, unilateral

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

remote effect of cancer on the nervous system

reticulum cell sarcoma

reversible neurologic disorder

sclerae, hyperpigmented

sclerosis, bone

screening

second wind phenomena

sedimentation rate, elevated

seizure

seizure, darkness induced

seizure, eye closure inducing

seizure, neonatal

seizure, neonatal abstenence syndrome

seizure, photosensitive

seizure, stimulus sensitive

selective serotonin reuptake inhibitors

sensorineural hearing loss

serotonin syndrome

serum alanine aminotransferase

sex reassignment surgery

skin, lesions in neurologic disorders

skin, thickened

skull x-ray, abnormal

skull x-ray, bony defect on

speech disorder, childhood

speech, delayed development of

speech, slowed

spina bifida

spinal cord, lesion of

stem cell transplantation

steroid therapy, CNS treatment and complications with

strychnine poisoning

stuporous

subarachnoid hemorrhage

subdural hematoma

substantia nigra

superior sagittal sinus thrombosis

third ventricle, mass of

thrombocytosis

toe walking

toilet seat neuropathy

tongue, black

tongue, discoloration

tongue, smooth

tongue, swelling

transgender

treatment of neurologic disorder

tremor

tremor, intention

trifluoperazine

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethoprim-sulfamethoxazole

urine osmolality, elevated

urine test in toxic screen

urine, dark

urticaria

uveitis

vascular endothelial growth factor

vegetarianism

very long chain fatty acids

viral infection

viral myopathy

Virchow-Robin spaces, dilated

vision, blurred

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual loss

visual loss, slow

vitamin B3, deficiency

vitamin deficiency

vitritis

vomiting, recurrent

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

Showing articles 0 to 50 of 96 Next >>

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Hyperpigmentation in Vitamin B12 Deficiency
NEJM 386:172, Sherman, S.V., 2022

Pain in Right Buttock after Carbon Monoxide Poisoning
BMJ 373:n1233, Hu, H. & Sun, Q., 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Clinicopathologic Conference, Primary Adrenal Insufficiency (Addisons Disease)
NEJM 376:1159-1167, Case 9-2017, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

A Young Woman with Blurred Vision and Distal Paresthesias
JAMA Neurol 72:1519-1523, Kung, N.H.,et al, 2015

A 12-Year Old Child with Fever, Headache, Shock and Coma
Lancet 385:576, Amores-Hernandez, I.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Hypernatremia
Adams & Victors Principles of Neurology Chp 40, pg 1148, Ropper, A.H.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Pellagra (Niacin, Nicotinic Acid, B3 Deficiency)
Adams & Victors Principles of Neurology Chp 41, pg 1170, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
AJNR 35:402-406, Bhargava, R.,et al, 2014

A 20-year-old Woman with Rapidly Progressive Weakness
Neurol 82:e200-e204, Paganoni, S.,et al, 2014

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Black Tongue Due to Adrenocortical Insufficiency
Arch Dis Child 97:1033, de Benedictis, F.M.,et al, 2012

Addisons Disease
Contemp Clin Dent 3:484-486, Sarkar, S.B.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010

Toxic and Drug-Induced Myopathies
JNNP 80:832-838, Dalakas,M.C., 2009

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Polyarteritis Nodosa Presenting as Rhabdomyolysis
J Korean Rheum Assoc Mar13(1):76-81, Bae,Y.D.,et al, 2006

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Rhabdomyolysis: An Evaluation of 475 Hospitalized Patients
Medicine 84:377-385, Melli,G.,et al, 2005

AAC/AHA/NHLBI Clinical Advisory on the Use and Safety of Statins
Stroke 33:2337-2341, Pasternak,R.C.,et al, 2002

Neurologic Presentation of Whipple Disease
Medicine 81:443-457, Gerard,A.,et al, 2002

Clinicopath Conf, Strychnine Poisoning, Case 12-2001
NEJM 344:1232-1239, , 2001

"Toilet Seat" Sciatic Neuropathy
Arch Neurol 56:116, Holland,N.R.,et al, 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Acute, Drug-Induced, Life-Threatening Neurological Syndromes
The Neurologist 4:196-210, Richard,I.H., 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Impaired Dark Adaptation in Symptomatic Carotid Artery Disease
Neurol 49:1353-1359, Havelius,U.,et al, 1997

Improved Dark Adaptation After Carotid Endarterectomy, Evidence of a Long-Term Ischemic Penumbra
Neurol 49:1360-1364, Havelius,U.,et al, 1997

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

Skin Lesions of the Spinal Axis and Spinal Dysraphism:Fifteen Cases & Review of the Literature
Arch Pediatr Adolesc Med 148:740-748, McAtee-Smith,J.,et al, 1994

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Showing articles 0 to 50 of 96 Next >>