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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 100 to 150 of 1679 << Previous Next >>

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Neurologic Manifestations of the Organoid Nevus Syndrome
Arch Neurol 42:236-240, Clancy,R.R.,et al, 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Human Growth Hormone & Creutzfeldt-Jakob Disease
Ann Int Med 103:288-289, Raiti,S., 1985

Creutzfeldt-Jakob Disease in a Young Adult with Idiopathic Hypopituitarism, Relation to Growth Hormone
NEJM 313:731-733, Koch,T.K.,et al, 1985

Clinical & Path Features & Lab Confirmation of Creutzfeldt-Jakob Disease with Pituitary Derived Human Growth Hormone
NEJM 313:734-738, Gibbs,C.J.,et al, 1985

Potential Epidemic of Creutzfeldt-Jakob Disease from Human Growth Hormone Therapy
NEJM 313:728-731, Brown,P.,et al, 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Schizencephaly:A Clinical & CT Study
Neurol 34:997-1001, Miller,G.M.,et al, 1984

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Precocious Puberty after Hypothalamic & Pituitary Irradiation in Young Children
NEJM 311:920-921, Brauner,R.,et al, 1984

Pergolide for the Treatment of Pituitary Tumors Secreting Prolactin or Growth Hormone
NEJM 309:704-709, Kleinberg,D.K.,et al, 1983

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
Neurol 33:1606-1609, Grunnet,M.L.,et al, 1983

Maternal Seizure Disorder, Outcome of Pregnancy, & Neurologic Abnormalities in the Children
Neurol 32:1247-1254, Nelson,K.B.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Sleep Apnoea in Acromegaly
BMJ 280:894-897, Perks,W.H.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Drug Therapy, Bromocriptine
NEJM 301:873-878, Parkes,D., 1979

Evaluation Of Acromegaly By Radioimmunoassay Of Somatomedin-C
NEJM 301:1138-1142, Clemmons,D.R.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Diagnostic Approaches to Pituitary Adenomas
Neurol 29:161-169, Drayer,B.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Disordered Growth Hormone & Prolactin Secretion in Primary Disorders of Sleep
Neurol 29:855-861, Clark,R.W.,et al, 1979

Computed Tomographic Scans, Cranial Irradiation & Endocrine Function
NEJM 299:100, Harrop,J.S., 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Chronic Hydrocephalus Associated with Short Stature & Growth Hormone Deficiency
Ann Neurol 2:246, Hier,D.B.,et al, 1977

Neurological Complications of Infantile Osteopetrosis
Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977

Central Pontine Myelinolysis
Quart J Med 45:373, Tomlinson,B.E.,et al, 1976

School Failure & Deafness After"Silent"Congenital Cytomegalovirus Infection
NEJM 295:468, Hanshaw,J.B.,et al, 1976

A Comparison of the Physical & Intellectual Development of Black Children with & without Sickle-Cell Trait
Pediatrics 56:1021, McCormack,M.K.,et al, 1975

Germinoma of third Ventricle (Case Record of MGH)
NEJM 293:653, Locke,S.,et al, 1975

Herpes Simplex & the Human Nervous System
Milit Med 140:765, Finelli,P.F., 1975

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Defects of Taste and Smell in Patients with Hypothyroidism
AmJMed 59:354-364, McConnell, R.J.,et al, 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Congenital Anomalies & Herpesvirus Infection
Am J Dis Child 126:364, Montogomery,J.R.,et al, 1973

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Microcephaly & Mental Retardation
Am J Dis Child 119:128, Martin,H.P., 1970



Showing articles 100 to 150 of 1679 << Previous Next >>