Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acromegaly
acromicria
Addison's disease
amenorrhea
amniocentesis
anatomy of
Angelman syndrome
ataxia
ataxia, progressive
behavior, combative
behavioral disorder
bromocriptine
cerebellar ataxia, primary
cerebellar degeneration
chromosome 15
cry, abnormal
cry, weak
Cushing's syndrome
developmental retardation
drooling
dwarfism
dysmorphic
eating disorder
electroencephalogram, abnormalities of
facial appearance, abnormal
failure to thrive
feeding disorder
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
growth hormone deficiency
hand flapping
headache
hirsutism
hyperphagia
hypodontia
hypogonadism
hypomyelination
hypopigmentation of skin
hypopituitarism
hypothyroidism
hypotonia
hypotonia, infants
imbalance
intellectual deficit
leukodystrophy
leukodystrophy, 4H
leukoencephalopathy
malformation, CNS, congenital
mental retardation
misdiagnosis
molecular genetics
MRI
MRI, abnormal
myopia
neoplasm, pituitary
neoplasm, pituitary, incidental
neoplasm, pituitary, treatment of
neuroendocrinology
neurologic disease, diagnoses of
obesity
octreotide
pituitary
pituitary stalk
pituitary, adenoma
pituitary, hormones of
pituitary, hyppoplasia
pituitary, microadenoma
plethora
posterior pituitary ectopia
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
progressive neurologic disorder
prolactin
prolactin, elevated
review article
seizure
sella turcica, hypoplasia of
short stature
somatostatin analogue
strabismus
suck, poor
teeth, abnormal
temper tantrums
tongue, protrusion of
treatment of neurologic disorder
tremulousness
visual field defect
white matter disease
wide based gait
Showing articles 1050 to 1100 of 1705 << Previous Next >>

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

Accelerated Aging of the Brain in Werner's Syndrome
Neurol 42:922-924, Kakigi,R.,et al, 1992

Cognitive Functioning in Cancer Patients:Effect of Previous Treatment
Neurol 42:434-436, Meyers,C.A.&Abbruzzese,J.L., 1992

Very Low Birth Weight and Growth to Age 8 years, Head Dimensions and Intelligence
Am J Dis Child 146:46-50, Kitchen,W.H.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

Cognitive and Motor Development in Infants at Risk for Human Immunodeficiency Virus
Am J Dis Child 146:218-222, Aylward,E.H.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Encephalitis in Cat Scratch Disease with Persistent Dementia
JNNP 55:133-135, Revol,A.,et al, 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Complications of Acute Stroke
Lancet 339:721-724, Oppenheimer,S.&Hachinski,V., 1992

Is Aluminium a Dementing Ion?
Editorial, Lancet 339:713-7141992., , 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

Effect of Cocaine Use On the Fetus
NEJM 327:399-407, Volpe,J.J., 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Vitamin B12 Metabolism in Multiple Sclerosis
Arch Neurol 49:649-652, Reynolds,E.H.,et al, 1992

Wernicke's Encephalopathy and Central Pontine Myelinolysis Associated with Hyperemesis Gravidarum
BMJ 305:517-518, Bergin,P.S.&Harvey,P., 1992

Plasma Vitamin B12 Level as a Potential Cofactor in Studies of HIV Type 1-Related Cognitive Changes
Arch Neurol 49:501-506, Beach,R.S.,et al, 1992

Excess Water Administration and Hyponatraemic Convulsions in Infancy
Editorial, Lancet, 339:153-155992., , 1992

Clinical Outcome in Aggressively Treated Meningeal Gliomatosis
Neurol 42:252-254, Grant,R.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Cerebral Infarction Associated with Protein C Deficiency
Stroke 23:108-111, Matsushita,K.,et al, 1992

Hypoglycemia Presenting as Basilar Artery Thrombosis
Stroke 23:112-113, Rother,J.,et al, 1992

Congenital Central Hypoventilation Syndrome:Diagnosis, Management, and Long-Term Outcome in Thirty-Two Children
J Pediatr 120:381-387, Weese-Mayer,D.E.,et al, 1992

Factors Impairing Daytime Performance in Patients with Sleep Apnea/Hypopnea Syndrome
Arch Int Med 152:538-541, Cheshire,K.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Pre-and Postcontrast MR Studies in Tuberous Sclerosis, Wippold
J Comput Assist Tomogr 16:69-72, II,F.J.,et al, 1992

Multiple Sclerosis Dementia
Neurol 42:696, Mendez,M.D.&Frey,W.F., 1992

Event-Related Potential P300 in MS, Relation to Magnetic Resonance Imaging and Cognitive Impairment
Arch Neurol 49:44-50, Honig,L.S.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
Neuroradiol 34:396-398, Aihara,M.,et al, 1992

Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections
Neuroradiology 33:239-242, Sugita,K.,et al, 1991

Accelerated Intracranial Occlusive Disease, Oral Contraceptives, and Cigarette Use
Neurol 41:1893-1901, Levine,S.R.,et al, 1991

Maternal Cocaine Abuse:The Spectrum of Radiologic Abnormalities in the Neonatal CNS
AJR 157:1105-1110, Heier,L.A.,et al, 1991

Prevention of Neural Tube Defects:Results of the Medical Research Council Vitamin Study
Lancet 338:131-137, 153-1541991., , 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease
J Pediatr 119:42-45, Riviello,J.J.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Defective Glucose Transport Across the Blood-Brain Barrier as Cause of Hypoglycorrhachia, Seizures, and Devel Delay
NEJM 325:703-709, 7311991., DeVivo,D.C.,et al, 1991

Clinical and Morphometric Analysis of the Hypoplastic Corpus Callosum
Arch Neurol 48:933-936, Schaefer,G.B.,et al, 1991

The Effect of Valproic Acid on Plasma Carnitine Levels
Am J Dis Child 145:9999-1001, Opala,G.,et al, 1991



Showing articles 1050 to 1100 of 1705 << Previous Next >>