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Differential
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Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
affect, inappropriate
asymptomatic
ataxia
attention deficit disorder with hyperactivity
behavioral disorder
blindness
bone marrow transplantation
children
cortical blindness
crying, pathologic
cultured skin fibroblasts
deafness
decerebrate posture
dementia
dementia, childhood
demyelinating disease
diet
dysarthria
dysarthria-clumsy hand syndrome
dysphagia
epidemiology of neurology
familial
fatty acid, elevated plasma content
gender
gene
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
hearing loss
hearing problems in children
hormone replacement
hyperpigmentation of skin
hypogonadism
intellectual deterioration
leukodystrophy
Lorenzo's oil
misdiagnosis
MRI
MRI, abnormal
MRI, spinal cord
multiple sclerosis, misdiagnosis
myelomalacia
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathy
neuropathy, peripheral
paraparesis
paraparesis, familial spastic
paraparesis, spastic
peroxisomal disease
personality change
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
pseudobulbar palsy
quadriparesis
review article
seizure
skin, darkening of
spinal cord, lesion of
spinal cord, pathologic exam of
testicular atrophy
treatment of neurologic disorder
very long chain fatty acids
visual loss
white matter disease
Showing articles 50 to 100 of 105 << Previous Next >>

MR Imaging of Adrenoleukodystrophy
Neuroradiology 33:25-29, Uchiyama,M.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy & Adrenomyeloneuropathy Present in the Same Family
Arch Neurol 47:665-669, Willems,P.J.,et al, 1990

Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow Transplant
NEJM 322:1860-1866, Aubourg,P.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
Roberts. R. G. , et al, Lancet 336:1523-1526., , 1990

Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
NEJM 320:138-142, Arahata,K.,et al, 1989

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

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Radiologic Screening for von Hippel-Lindau Disease:Role of Gd-DTPA Enhanced MR Imaging of the CNS
J Comput Assist Tomogr 13:743-755, Filling-Katz,M.R.,et al, 1989

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Dietary Erucic Acid Therapy for X-Linked Adrenoleukodystrophy
Neurol 39:1415-1422, Rizzo,W.B.,et al, 1989

MRI Detects Cerebral Involvement in Neurologically Asymptomatic Patients with Adrenoleukodystrophy
Neurol 39:1619-1621, Aubourg,P.,et al, 1989

Duchenne Muscular Dystrophy Carrieris
Neuroradiology 31:373-376, Matsumura,K., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Atypical CT Scans in Adrenoleukodystrophy
J Comput Assist Tomogr 11:333-336, Hong-Mango,E.T.,et al, 1987

Preventive Screening for the Fragile X Syndrome
NEJM 315:607-609, Turner,G.,et al, 1986

Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985

Adrenoleukodystrophy:Early Frontal Lobe Involvement on Computed Tomography
J Comput Assist Tomogr 8:128-130, MacDonald,J.T.,et al, 1984

Duchenne Muscular Dystrophy:Carrier Detection by Ultrasound & Computerised Tomography
Lancet 2:1199-1200, Rott,H., 1983

Evoked Response Studies in Patients with Adreno-leukodystrophy & Heterozygous Relatives
Arch Neurol 40:356-359, Garg,B.P.,et al, 1983

Nuclear Magnetic Resonance (NRM) Imaging in White Matter Dis. of the Brain Using Spin-Echo Sequences
J Comput Assist Tomogr 7:290-294, Young,I.R.,et al, 1983

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts & Correlation with Disease Expression
Neurol 32:540-2, O'Neill,B.P.,et al, 1982

Detection Of Adrenoleucodystrophy Carriers By Means Of Evoked Potentials
Lancet 2:852-853, Moloney,J.B.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Adrenoleukodystrophy, Unusual Computed Tomographic Appearance
Arch Neurol 39:782-783, Young,R.S.K.,et al, 1982

Familial X-linked Addison Dise. as an Expression of Adrenoleukodystr. :C26 Fatty Acid in Cult. Skin Fibroblasts
Neurol 32:543-547, O'Neill,B.P.,et al, 1982

The Adrenoleukomyeloneuropathy Complex:Expression in Four Generations
Neurol 31:151-156, O'Neill,B.P.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Adrenoleukodystrophy:Increased Plasma Content of Saturated Very Long Chain Fatty Acids
Neurol 31:1241-1249, Moser,H.W.,et al, 1981

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Skin & Conjunctival Nerve Biopsies in Adreno-leukodystrophy & Its Variants
Ann Neurol 8:291-295, Martin,J.J.,et al, 1980

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts
Ann Neurol 7:542-549, Moser,H.W.,et al, 1980

Adrenoleukodystrophy. Report of Two Cases With Relapsing & Remitting Courses
Arch Neurol 37:448-450, Walsh,R., 1980

Kluver-Bucy Syndrome Caused by Adreno-leuko-dystrophy
Neurol 30:1131-1132, Powers,J.M.,et al, 1980

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

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Brainstem Auditory Evoked Response in Adrenoleukodystrophy
Ann Neurol 6:269-270, Black,J.A.,et al, 1979

Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979

Brainstem Auditory Evoked Responses in Leukodystrophies
Neurol 29:1089-1093, Ochs,R.,et al, 1979



Showing articles 50 to 100 of 105 << Previous Next >>