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Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal migraine

abscess, sphenoid sinus

acanthosis nigricans

Addison's disease

adrenal crisis, acute

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

affect, inappropriate

Albright disease

alcohol, neurologic complications with

anemia, megaloblastic

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiography, cerebral

angiography, posterior fossa

angiography, vertebral artery

anorexia nervosa

anterior horn cell disease

arterial dissection

arterial dissection, aorta

arterial dissection, basilar

arterial dissection, bilateral

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, vertebral

arteritis, temporal

ataxia telangiectasia

ataxia, cerebellar

autoimmune disease

autonomic dysfunction

B 12 deficiency

B 12 deficiency, infants

bacterial infection

bacterial infection, CNS

Bannayan-Riley-Ruvalcaba syndrome

basal ganglia, calcification of

behavior, combative

behavioral disorder

bladder dysfunction

bone marrow biopsy

bone marrow transplantation

bone survey, metastatic

brain scan, abnormal

brainstem, infarction of

bulimia nervosa

burning paresthesia

calcification, intracranial

carbon monoxide poisoning

carcinoma of lung

carpal tunnel syndrome

Castleman's disease

CAT scan, abnormal

CAT scan, angiography

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, disappearing lesion on

CAT scan, orbits

cavernous sinus, syndrome

cecum perforation

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

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

chemotherapy, CNS treatment and complications with

chorionic gonadotropin

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

Cockayne's syndrome

coenzyme Q10 deficiency

cogwheel rigidty

collagenous sprue

color vision, impaired

compression fracture

confusional state, acute

congenital malformation

contractures, joint

cortical blindness

cotton-wool spots

cranial nerve palsies

cranial nerve palsy, alternating

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

cyclic vomiting

cyclic vomiting syndrome

cyst, parenchymal

decerebrate posture

delay in diagnosis

dementia, childhood

demyelinating disease

dermal sinus tract

dermatitis herpetiformis

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diagnostic criteria

diastematomyelia

differential diagnosis

disability, neurological

doppler, transcranial

drug interactions

duplex ultrasound

dyschromatopsia

dysraphism, spinal

eating disorder

ectopic pinealoma

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electrophoretic pattern, serum

emergencies, neurologic

emotional lability

encephalomyopathy

encephalopathy, post anoxic

endocarditis, infectious

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

epidermal nevus syndrome

erythromelalgia

ethylene glycol

exercise intolerance

eye movement, disorders of

eye movement, painful

face, numbness of

facial anomalies

facial appearance, abnormal

facial nerve palsy

facial pain, atypical

fatty acid, elevated plasma content

fibrous dysplasia

fibrous dysplasia of orbit

finger swelling

fingernails, abnormal

fingernails, white

fingers, abnormal

folic acid deficiency

follicle stimulating hormone

fracture, long bone

fundus, abnormality of

fungal infection

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glossopharyngeal nerve

glossopharyngeal neuralgia

glucose tolerance test, abnormal

gram positive rod

growth retardation

hair, darkening of

headache, positional

headache, recurrent

headache, severe

hemangioma, leptomeningeal

hemifacial atrophy

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes simplex virus, human nervous system and

herpes simplex, neurocutaneous lesions in

heterochromia iridis

hormone replacement

hormone therapy

Horner's syndrome

Horner's syndrome, etiologies of

hyperbaric oxygen

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hypoalbuminemia

hypoglycemic coma

hyponatremic encephalopathy

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hypotension, systemic

hypothalamus, disturbance of

hypothalamus, neoplasm of

hypothermia, causes of

hypotonia, infants

IgG4-related disease

immunoelectrophoresis, serum

immunosuppressive agents

implant contraceptives

inappropriate antidiuretic(A.D.H.)hormone

inclusion bodies

inclusion bodies, intracytopasmic

incontinentia pigmenti

insulin resistance

intellectual deficit

intellectual deterioration

intestinal biopsy

intracranial hypertension, benign

intracranial pressure, increased

lactic acidemia

lactic dehydrogenase(LDH)

lateral rectus palsy

leukoencephalopathy

leukoencephalopathy, toxic

level of consciousness, decreased

liver transplantation

luteinizing hormone

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoid hyperplasia

lymphoma involving CNS

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Marcus Gunn pupil

McCune-Albright syndrome

memory, impairment of

mental retardation

mental status, abnormal

methylmalonic acid, serum

migraine, children

migraine, equivalents

mitochondrial disease

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

movement disorder

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, spinal cord

multiple myeloma

multiple sclerosis

muscle weakness

myeloma, osteosclerotic

myocardial infarction

nasal stuffiness

nausea and vomiting

neoplasm, pituitary

nephrotic syndrome

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

night blindness

nutritional deficiency

oculocutaneous albinism

oculomasticatory myorhythmia

ophthalmoplegia

ophthalmoplegia, painful

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, enhancement

optic nerve, lesion of

optic neuropathy

orange peel appearance of skin

orbit, inflammation in

orbit, lesions of

otitis, neurologic complications with

pain, abdominal

pain, periorbital

papilledema, unilateral

paradichlorobenzene

paraparesis, spastic

paratrigeminal syndrome

paresthesias, hands

Parkinsonism syndrome

PAS positive material in the brain

penis, pigmented macules

peripheral blood smear, abnormal

peripheral pulse, absent

pernicious anemia

peroxisomal disease

personality change

photosensitivity, skin

physical therapy

pigmentary retinopathy

pigmented macules

pituitary, adenoma

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pleural effusion

polycythemia, primary

polycythemia, secondary

polymerase chain reaction

polymyalgia rheumatica

polyps, gastrointestinal tract

port wine nevus

post herpetic neuralgia

posterior column disease

posterior inferior cerebellar artery syndrome

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

progressive neurologic disorder

prolactin, elevated

protease inhibitor, HIV-1

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, unilateral

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

radiation therapy, CNS treatment and complications with

Raynaud's phenomenon

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

refractory sprue

remote effect of cancer on the nervous system

respiratory tract infection

reticulum cell sarcoma

retinal hemorrhages

retro-orbital pain

sclerosis, bone

sedimentation rate, elevated

sensorineural hearing loss

shock, hypovolemic

silver toxicity

sinuses, diseases of

skin, cherry-red

skin, darkening of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skin, thickened

skull x-ray, abnormal

skull x-ray, bony defect on

spinal cord, lesion of

stem cell transplantation

steroid therapy, CNS treatment and complications with

stress, emotional

Sturge-Weber syndrome

subarachnoid hemorrhage

superior sagittal sinus thrombosis

sweating, abnormality of

sympathetic block

syphilis, neurologic complications with

systemic illness

testicular atrophy

testicular biopsy

tethered spinal cord

third ventricle, mass of

thrombocytopenia

tongue, discoloration

tongue, swelling

treatment of neurologic disorder

tremor, intention

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethoprim-sulfamethoxazole

tropical disease

ultrasonography

urinalysis, abnormal

urine osmolality, elevated

vascular endothelial growth factor

very long chain fatty acids

viral infection

Virchow-Robin spaces, dilated

vision, blurred

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual loss, progressive

visual loss, slow

vitamin B3, deficiency

vitamin deficiency

vomiting, recurrent

walking, difficulty with

weakness, generalized

Whipple's disease

white matter disease

x-ray, lumbar spine

Showing articles 0 to 50 of 1355 Next >>

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

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

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

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

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

Peripheral Neuropathy Associated with Silver Toxicity
Neurol 92:481-483, Naddaf, E.,et al, 2019

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

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

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

Poor Vision in a Patient with White Hair and Pale Skin
BMJ 352:i24, Tripathy, K. & Sharma, Y.R., 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

Clinicopathologic Conference, Ethylene Glycol Ingestion
NEJM 372:465-473, Case 4-2015, 2015

The Acquired Metabolic Disorders of the Nervous System, Carbon Monoxide Poisoning
Adams & Victors Principles of Neurology Chp 40, pg 1138, 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

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

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

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

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

Clinicopath Conf., Allergic Fungal Sinusitis
NEJM 359:2825-2833, Case 40-2008, 2008

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

A Tourist With Dengue Fever and Visual Loss
Lancet 360:1070, Haritoglou,C.,et al, 2002

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

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

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

Extracranial and Intracranial Vertebrobasilar Dissections:Diagnosis and Prognosis
JNNP 63:46-51, deBray,J.M.,et al, 1997

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 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

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Pituitary Adenoma in McCune-Albright Syndrome:MR Demonstration
J Comput Assist Tomogr 13:685-688, O'Laughlin,R.L.,et al, 1989

Brain Malformations in Linear Nevus Sebaceous Syndrome:An MR Study
J Comput Assist Tomogr 12:338-340, Sarwar,M.&Schafer,M.E., 1988

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Clinicopath Conf
Castleman's Disease, Synd of Polyneuropathy, Organomegally, Endocrinopathy, Monoclonal Gammopathy, &, Skin CPOEM Synd),NEJM 316:606-618,1987., 1987

Peripheral Neuropathy Associated with Dysproteinaemia, Skin Changes, & Endocrinopathy
BMJ 292:1415-1416, Burton,J.L., 1986

Osteosclerotic Myeloma & Peripheral Neuropathy
Neurol 33:202-210, Kelly,J.J.,et al, 1983

Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
Medicine 59:311-322, Bardwick,P.A., 1980

Clinical Pathological Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 18-1979, NEJM 300:1037-104579., , 1979

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Showing articles 0 to 50 of 1355 Next >>