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Differential
(Click to cross reference)
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
false negative
genetic testing
Notch3 gene
Notch3 gene, false negative
Showing articles 3050 to 3100 of 3323 << Previous Next >>

Benign Recurrent Aseptic Meningitis (Mollaret's Meningitis)
Arch Neurol 36:657-658, Galdi,A.P., 1979

Familial Arteriovenous Malformation
Ann Neurol 5:585-587, Snead,O.C.III.,et al, 1979

Clinical Pathological Conference
Herpes Simplex Encephalitis, Case Record 44-1979, NEJM 301:987-994979., , 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Cytomegalovirus Infection of the Adult Nervous System
Ann Neurol 5:458-461, Duchowny,M.,et al, 1979

Human-To-Human Transmission of Rabies Virus by Corneal Transplant
NEJM 300:603-604, Houff,S.A.,et al, 1979

Escherichia Coli Meningitis with Features of Acute Hemorrhagic Leukoencephalitis
abstract. J Neuropath Exper Neurol 38:3351979., Pogacar,S.,et al, 1979

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Helper & Suppressor T-Lymphocyte Leukemia In Ataxia Telangiectasia
NEJM 300:700-704, Saxon,A.,et al, 1979

Computerized Tomography in Hereditary Nonprogressive Chorea
Arch Neurol 36:249-250, Rice,E.,et al, 1979

Familial Tourette Syndrome
Ann Neurol 5:104, Guggenheim,M.A., 1979

Familial Lumbar Spinal Stenosis with Acute Disc Herniation, Case Reports of Four Brothers
J Neurosurg 51:234-236, Varughese,G.,et al, 1979

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
NEJM 301:588-590, Askanas,V.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Nervous System Complication of Herpes Zoster:Immunofluor Demonstrat of Varicellazoster Antigen in CSF Cells
JNNP 42:452-457, Peters,A.C.B., 1979

CNS Listeriosis, Rhomboencephalitis in a Healthy, Immunocompetent Person
Arch Neurol 36:513-514, 1979, Katz,R.I.,et al, 1979

Salmonella Meningitis
Arch Neurol 36:578-580, Kauffman,C.A.,et al, 1979

Clinical Pathological Conference
Candida Endocarditis with Cerebral Embolism, Case 27-1979, NEJM 301:34-42979., , 1979

Neurological Manifestations & Mycoplasma Pneumoniae Infection
BMJ 2:832-833, Hodges,G.R.,et al, 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Familial Kearns-Sayre syndrome
Neurol 29:1172-1174, Schnitzler,E.R.,et al, 1979

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

Famillial Carpal Tunnel Syndrome
Arch Neurol 36:727, Massey,E.W., 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Familial Fatal Parkinsonism with Alveolar Hypoventilation & Mental Depression
Ann Neurol 6:523-531, Purdy,A.,et al, 1979

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

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

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Transient Cerebral Dysfunction Following Chemotherapy for Osteogenic Sarcoma
Ann Neurol 3:441, Allen,J.C.,et al, 1978

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Familial Hypopituitarism with Large Sella Turcica
NEJM 298:698, Parks,J.S.,et al, 1978

Trypanosoma Cruzi in the Cerebrospinal Fluid During the Acute State of Chagas'Disease
NEJM 298:604, Hoff,R.,et al, 1978



Showing articles 3050 to 3100 of 3323 << Previous Next >>