Differential (Click to cross reference) advances in neurology akinetic mute Alzheimer's disease Alzheimer's disease, early onset Alzheimer's disease, familial Alzheimer's disease, familial, late onset apolipoprotein E APP ataxia ataxia, cerebellar ataxia, progressive brainstem, atrophy CAG repeats cerebellar ataxia, hereditary cerebellar atrophy, primary cerebellar vermis cerebral cortex cerebral palsy children chromosomal abnormality chromosome 1 chromosome 14 chromosome 21 Clinical Pathologic Conference(C.P.C.) deep gray nuclei degenerative diseases of CNS dementia dementia, presenile dementia, rapidly progressive depression dexterity, impaired diurnal variation dopa responsive dystonia dysarthria dystonia dystonia, etiology of dystonia, painful familial gait disorder gene gene mutation genetic counselling genetic linkage genetic neurologic disorders genetic testing Gerstmann-Straussler-Scheinker disease headache heralding manifestation L-dopa leg spasms leg spasms, painful misdiagnosis molecular genetics movement disorder MRI MRI, abnormal MRI, diffusion weighted neurologic disease, diagnoses of neurologic signs obsessive-compulsive disorder oculopharyngeal muscular dystrophy old age, neurology of pain Parkinson disease, differential diagnosis of Parkinsonism syndrome presenilin-1 gene presenilin-2 gene prion disease prion protein gene prognosis progressive neurologic disorder protein 14-3-3, cerebrospinal fluid psychiatric problems in neurologic disorders reversible neurologic disorder review article short stature sinemet spinocerebellar ataxia spinocerebellar ataxia type 1 spinocerebellar ataxia type 14 spinocerebellar ataxia type 3/Machado Joseph disease spinocerebellar degeneration tandem gait, ataxic toe walking treatment of neurologic disorder tremor tremor, postural trinucleotide repeats walking, difficulty with wheelchair

Showing articles 1350 to 1362 of 1362 << Previous Ocular Myopathy Arch Neurol 20:1, Magora,A.,et al, 1969 The Oculopharyngeal Syndrome JAMA 203:1003, Murphy,S.F.,et al, 1968 Myopathy of the Quadriceps Muscles J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968 Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J. Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968 Huntington's Chorea Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968 Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both NEJM 274:384, Renuart,A., 1966 Inherited Aminoacidopathies Demonstrating Vitamin Dependency NEJM 281:145, Rosenberg,L., 1965 Morquio's Disease, A Radiologic & Morphologic Study Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964 Familial and Conjugal Multiple Sclerosis Brain 86:315-332, Schapira,K.,et al, 1963 The Cornelia de Lange Syndrome J Pediatr 63:1000-1020, Ptacek,L.J., 1963 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Microcephaly Arch Dis Child 37:623-627, Davies,H.,et al, 1962 Clinical Study of Nine Patients with ReNU Syndrome , Okamoto,N.,et al, Showing articles 1350 to 1362 of 1362 << Previous