Neudle.com: ataxia congenital

Differential
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abdominal protrusion

abortion, spontaneous

acanthocytosis

agenesis of aqueduct of Sylvius

alpha-fetoprotein

aneurysm

aneurysm, asymptomatic

aneurysm, intracranial

angiography, cerebral

aniridia

anterior tibial muscle weakness

antibodies to voltage-gated calcium channels

apraxia of eye movements

aqueduct of Sylvius, stenosis

ataxia telangiectasia

bacterial endocarditis, neurologic manifestations of

Balint's syndrome

Bassen-Kornzweig syndrome

bulbar palsy, progressive

calcification, intracranial

calcification, periventricular

calcium channel dysfunction

carcinoembryonic antigen

CAT scan, emission, abnormal

cataracts

cataracts, congenital

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, bilateral

children

chloride channel dysfunction

chorea

choreoathetosis

chorioretinitis

chromosomal abnormality

chromosome 11

Clinical Pathologic Conference(C.P.C.)

Coats syndrome

Cockayne's syndrome

coma

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital myopathy

congenital paresis

consanguinity

contactin associated protein like 1 antibodies

contactin associated protein like 1 auto antibodies.(CNTN1)

Dandy Walker malformation

Dandy Walker malformation, adult

deafmute

deafness

degenerative diseases of CNS

dementia

dental procedure, neurologic complications with

diabetes mellitus

difficulty climbing stairs

distal muscle weakness

electroencephalogram, abnormalities of

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

endovascular therapy

eye movement, disorders of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

familial

familial hemiplegic migraine

gammaglobulin therapy, intravenous, refractory

genetic neurologic disorders

hematoma, intracerebral

hepatosplenomegaly

herpes simplex virus

histochemistry of muscle

Hurler's syndrome

hydranencephally

hydrocephalus

hydrocephalus, congenital

hydrocephalus, non-communicating(obstructive)

hydrocephalus, treatment of

hypokalemic periodic paralysis

intellectual deterioration

intracerebral hemorrhage

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

iris, abnormal

jittery baby

juvenile paresis

Kearns-Sayre syndrome

keratoconus

Laurence-Moon-Bardet-Biedl syndrome

leukemia

lid closure, weakness of

lymphocytic choriomeningitis

lymphoma

maculopathy

malformation, CNS, congenital

malignant hyperpyrexia

Marinesco-Sjogren syndrome

mitral valve prolapse

mitral valve regurgitation

monoclonal gammopathy

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

mucopolysaccharidoses

multiple system atrophy

mumps virus

muscle biopsy

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal infection, viral

neuritis

neurocutaneous disease

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuropathology

neuropathology, brain

neuropathy

neuropathy, autoimmune

nodopathy, autoimmune

nystagmus

obesity

occipital lobe, infarction

occipital lobe, infarction, bilateral

ocular motility, disorders of

ocular myopathy

old age, neurology of

paramyotonia congenita

paraspinal muscle

paraspinal muscle weakness

parietal lobe, infarction

paroxysmal neurologic deficits

pleocytosis of cerebrospinal fluid

polydactyly

Poretti-Boltshauser syndrome

posterior cerebral artery occlusion

posterior fossa, lesion of

potassium channel antibodies

potassium channel dysfunction

progeria

prognosis

progressive neurologic disorder

pseudoaneurysm

pseudoretinitis pigmentosa

psychiatric disorder

psychomotor retardation

radiation hypersensitivity

rapidly progressing neurologic illness

rubella encephalitis, progressive

serologic testing of cerebrospinal fluid

shunt procedure, ventricular

shunt procedure, ventriculo-peritoneal

simultanagnosia

skin, lesions in neurologic disorders

sloped shoulders

slow virus infection of CNS

sodium channel dysfunction

spasticity

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 6

standing difficulty

stem cell transplantation

stooped posture

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

superior cerebellar artery infarction

transplacental virus infections

transverse smile

treatment of neurologic disorder

visual fields, constricted

visual loss

walking, difficulty with

weakness

weakness, progressive

Showing articles 950 to 1000 of 2289 << Previous Next >>

Should We Screen for Familial Intracranial Aneurysm?
Stroke 30:312-316, Crawley,F.,et al, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

Treatment of Intracranial Aneurysms by Embolization with Coils,A Systematic Review
Stroke 30:470-476, Brilstra,E.H.,et al, 1999

Validity of Prediction of the Site of Ruptured Intracranial Aneurysms with CT
Neurol 52:34-39, van der Jagt,M.,et al, 1999

Risk of Cerebral Angiography in Patients with Subarachnoid Hemorrhage,Cerebral Aneurysm,and Arteriovenous Malformation,A Meta-Analysis
Stroke 30:317-320, Cloft,H.J.,et al, 1999

Assessment of the Value of MR Imaging for Examining Patients with Angiographically Negative Subarachnoid Hemorrhage
AJR 172:201-206, Rogg,J.M.,et al, 1999

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Unruptured Intracranial Aneurysms - Risk of Rupture and Risks of Surgical Intervention
NEJM 339:1725-1733,1774, The Internat'l Study of Unruptured Intracranial An, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Risk of Recurrent Subarachnoid Hemorrhage After Complete Obliteration of Cerebral Aneurysms
Stroke 29:2511-2513, Tsutsumi,K.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Terson Syndrome:CT Evaluation in 12 Patients
AJNR 19:743-747, Swallow,C.E.,et al, 1998

Small Retinal Hemorrhages as the Only Sign of an Intracranial Aneurysm
Am J Ophthalmol 125:401-403, Kiriakopoulos,E.T.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Double-Blind Randomized Trial of Tramadol for the Treatment of the Pain of Diabetic Neuropathy
Neurol 50:1842-1846, Harati,Y.,et al, 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Subarachnoid Hemorrhage:Aneurysm Detection ahnd Preoperative Evaluation with CT Angiography
Radiology 208:423-430, Velthuis,B.K.,et al, 1998

Imaging of the Peripheral Nervous System:Evaluation of Peripheral Neuropathy and Plexopathy
AJNR 19:1011-1023, Maravilla,K.R.&Bowen,B.C., 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Dilemma of Discontin of Anticoag Therapy for Pts with Intracran Hem & Mech Heart Valves
Neurosurg 42:769-773, Eelco,F.M.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Neurologic Outcomes in Children with Post-Pump Choreoathetosis
J Pediatr 132:162-164, Holden,K.R.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Dyslexia
NEJM 338:307-312, Shaywitz,S.E., 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Metabolic Abnormalities in Development Dyslexia Detected by 1H Magnetic Resonance Spectroscopy
Lancet 351:1849-1852, Rae,C.,et al, 1998

Calcium Antagonists in Patients with Aneurysmal Subarachnoid Hemorrhage
Neurol 50:876-883, Feigin,V.L.,et al, 1998

Quality of Life in Patients and Partners After Aneurysmal Subarachnoid Hemorrhage
Stroke 29:798-804, Hopp,J.W.,et al, 1998

Prevent of a 1st Stroke by Transfusions in Children/Sickle Cell Anemia & Abnorm Results on Transcr Doppler Ultrasonog
NEJM 339:5-11, Adams,R.J.,et al, 1998

Stroke in Children and Sickle-Cell Disease, Baltimore-Washington Cooperative Young Stroke Study
Neurol 51:169-176, Earley,C.J.,et al, 1998

Clinical Features of Moyamoya Disease in the United States
Stroke 29:1347-1351, Chiu,D.,et al, 1998

Mortality and Morbidity of Surgery for Unruptured Inracranial Aneurysms
Stroke 29:1531-1538, Raaymakers,T.W.M.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Intracerebral Haemorrhage Caused by Drug Abuse
Lancet 351:1029, McEvoy,A.W.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Showing articles 950 to 1000 of 2289 << Previous Next >>