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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 50 to 100 of 1679 << Previous Next >>

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Creutzfeldt-Jakob Disease from Contaminated Growth Hormone Extracts in France
Neurol 47:690-695, Billette de Villemeur,T.,et al, 1996

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Benign Intracranial Hypertension in Children with Growth Hormone Deficiency Treated with Growth Hormone
J Pediatr 126:996-999, Malozowski,S.,et al, 1995

Effect of Octreotide, A Somatostatin Analog, on Sleep Apnea in Patients with Acromegaly
Ann Int Med 121:478-483, Grunstein,R.R.,et al, 1994

Timing of Vulnerability of the Brain to Iodine Deficiency in Endemic Cretinism
NEJM 331:1739-1744, 17701994., Xue-Yi,C.,et al, 1994

Acromegaly:Clinical and Biochemical Features in 500 Patients
Medicine 73:233-240, Ezzat,S.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Growth Hormone, Insulin-Like Growth Factor I, and Benign Intracranial Hypertension
NEJM 329:665-666, Malozowski,S.,et al, 1994

Fetal Alcohol Syndrome and Fetal Alcohol Effects
Comm of Substance Abuse & Comm on Children with Disabilitites, Pediatrics 91:1004-100693., , 1993

Prenatal Alcohol Exposure and Long-Term Developmental Consequences
Lancet 341:907-910, Spohr,H.,et al, 1993

Hypopituitarism After Tuberculous Meningitis in Childhood
Ann Int Med 118:701-706, Lam,K.S.L.,et al, 1993

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Acromegaly:Treatment After 100 Years
BMJ 307:1505-1506, Wass,J.A.H., 1993

Hypothalamic-Pituitary Dysfunction after Radiation for Brain Tumors
NEJM 328:87-94, Constine,L.S.,et al, 1993

Octreotide Treatment of Acromegaly, A Randomized, Multicenter Study
Ann Int Med 117:711-718, Ezzat,S.,et al, 1992

MRI of the Pituitary Area in Children Treated for Acute Lymphobl Leuk with Low-Dose (18-Gy) Cranial Irradiation
Am J Dis Child 146:1343-1348, Cicognani,A.,et al, 1992

"Friendly Fire"in Medicine:Hormones, Homografts, and Creutzfeldt-Jakob Disease
Lancet 340:24-27, Brown,P.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
J Pediatr 120:740-746, Autti-Ramo,I.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Sleep Apnea in Acromegaly
Ann Int Med 115:527-532, Grunstein,R.R.,et al, 1991

Cerebral Infarction in Young People, A Study of 148 Patients with Early Cerebral Angiography
JNNP 54:576-579, Lisovoski,F.&Rousseaux,P., 1991

Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
Lancet 337:1441-1442, Collinge,J.,et al, 1991

Mortality, Neoplasia, & Creutzfeldt-Jakob Disease in Patients Treated with Human Pituitary Growth Hormone in the UK
BMJ 302:824-828, Buchanan,C.R.,et al, 1991

Effect of Very Low Brith Weight and Subnormal Head Size on Cognitive Abilities at School Age
NEJM 325:231-237, Hack,M.,et al, 1991

Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States
JAMA 265:880-884, Fradkin,J.E.,et al, 1991

Diagnosis and Management of Hormone-Secreting Pituitary Adenomas
NEJM 324:822-831, Klibanski,A.&Zervas,N.T., 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
JAMA 264:605-609, 6221990., Yamazaki,J.N.&Schull,W.J., 1990

Acromegaly
NEJM 322:966-977, Melmed,S., 1990

Acromegaly in an Infant
Pediatrics 83:998-1002, Blumberg,D.L.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Pediatric Acquired Immunodefieiency Syndrome
Am J Dis Child 142:29-35, Belman,A.L.,et al, 1988

Human Growth Hormone Therapy & Creutzfeldt-Jakob Disease:A Drama in Three Acts
Pediatrics 81:85-92, Brown,P., 1988

Difference Between Herpes Simplex Virus Type I & Type 2 Neonatal Encephalitis in Neurological Outcome
Lancet 1:1-4, Corey,L.,et al, 1988

The Decline and Fall of Creutzfeldt-Jakob Disease Associated with Human Growth Hormone Therapy
Neurol 38:1135-1137, Brown,P., 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Isolated Growth Hormone Deficiency after Cerebral Edema Complicating Diabetic Ketoacidosis
NEJM 316:857-859, Keller,R.J.&Wolfsdorf,J.I., 1987

Pituitary Growth Hormone from Human Cadavers:Neurologic Disease in Ten Recipients
Neurol 37:1211-1213, Rappaport,E.B.&Graham,D.J., 1987

Iatrogenic Creutzfeldt-Jakob Disease
Neurol 37:1520-1522, Rappaport,E.B., 1987

Does Growth Hormone Cause Relapse of Brain Tumors
Lancet 1:711-713, Clayton,P.E.,et al, 1987



Showing articles 50 to 100 of 1679 << Previous Next >>