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Differential
(Click to cross reference)
acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
adrenal mass
advances in neurology
Alzheimer's disease
amniocentesis
amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
areflexia
arrhythmia, cardiac
astrocytoma
ataxia
atrial myxoma
autonomic dysfunction
cafe au lait spots
carcinoma
cardiomyopathy
CAT scan, abdomen
CAT scan, abnormal
cataracts
catecholamine
cavernous hemangioma
cerebral embolism
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, young adult
children
chromosomal abnormality
chromosome 17
chromosome 22
coagulopathy
constipation
cranial nerve tumor
deafness
developmental retardation
differential diagnosis
DNA probes
Ehlers-Danlos syndrome
ependymoma
Fabry's disease
familial
fibromuscular dysplasia
gadolinium
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
hamartoma
headache
hearing loss
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
homocystinuria
Huntington's chorea
hypertension
intellectual deficit
intracerebral hemorrhage
intracerebral hemorrhage, young adult
iris, abnormal
karyotyping
learning disability
learning disability, in children
Legius syndrome
life expectancy
Lisch nodules
long bone lesion
lymphoma
macrocephaly
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
meningioma
meningioma, familial
meningioma, multiple
merlin
migraine
migraine, hemiplegic
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
moyamoya
MRI
MRI, abnormal
MRI, spine
multiple endocrine neoplasia
muscular dystrophy
muscular dystrophy, Duchenne
myotonia dystrophica
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-familial occurrence
nerve growth factor
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic disease, diagnoses of
neurologic signs
neuropathy
NF1 gene
optic glioma
palpitations
patient information and support
pheochromocytoma
polycythemia, primary
precocious puberty
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
protein C deficiency
pruritus
pseudarthrosis
pseudoxanthoma elasticum
recombinant DNA
review article
RFLPs
Riley-Day syndrome
root lesion, nerve
schwannoma
scoliosis
seizure
sensory ganglia
sensory ganglia, abnormal
Shy-Drager syndrome
sickle cell disease
skin, lesions in neurologic disorders
skull x-ray, abnormal
skull x-ray, bony defect on
slit lamp examination
speech disorder
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary intradural
spinal cord, neoplasm, intramedullary
spinal cord, neoplasm, neurofibroma
SPRED1 mutation
sweating
thrombocytopenia
tinnitus
treatment of neurologic disorder
tuberous sclerosis
urinary catecholamines
Von Hippel Lindau
web sites
weight loss
white freckles
Showing articles 1700 to 1738 of 1738 << Previous

Teratogenic Effect of Anticonvulsnats
Lancet 198, 1973 Jan., , 1973

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973

Ataxia-Telangiectasia-Clonal Growth of Translocation Lymphocytes
NEJM 289:286, Hecht,F.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

Familiar Basilar Impression
Neurol 22:554, Paradis,R.,et al, 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Case Records of MGH
NEJM 287:1033, 1972 Choroid Plexus Papillary Tumor., , 1972

Dumbbell Anterolateral Spinocranial Neurofibroma with a Note on Thigh Muscle Atrophy & Fasciculation
Neurochir 4:143, Bartal,A.D.,et al, 1972

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Endocrine Disorders Associated with the Phakomatoses
Handbook of Clinical Neurology 14:731-758, Bricaire,H.,et al, 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

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

Myasthenia Gravis & Hyperthyroidism Occurring in Two Sisters
Neurol 21:377, Namba,T.,et al, 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Polyneroupathies of Undetermined Cause
Acta Neurol Scand (Supp) :5970., Prineas,J., 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

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

Optic Glioma of Childhood
Br J Ophthalmol 53:793, Hoyt,W.&Baghdassarian,S., 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,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

The Brain in Multiple Neurofibromatosis:A Suggested Neuropathological Basis for the Assoc. Mental Defect
Brain 90:829, Rosman,N.P.,et al, 1967

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

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Familial and Conjugal Multiple Sclerosis
Brain 86:315-332, Schapira,K.,et al, 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

Neuro CPC of MGH
Enteric Cyst of Cervical Spinal Canal, NEJM 262:623-6271960., , 1960

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,



Showing articles 1700 to 1738 of 1738 << Previous