Neudle.com: ptosis familial

Differential
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abdominal distention

abducens nerve paralysis

altered states of consciousness

alveolar hypoventilation

autonomic dysfunction

baldness

blood dyscrasias, neurologic findings with

brainstem, dysfunction

cachexia

calcification, intracranial

CAT scan, false negative

cataracts

central core disease

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

children

chromosome 19

chronic progressive external ophthalmoplegia

cleft palate

Clinical Pathologic Conference(C.P.C.)

coma

congenital heart disease

congenital malformation

congenital myasthenic syndromes

congenital myopathy

consanguinity

cough

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

dementia

developmental retardation

diarrhea

diplopia

distal muscle weakness

electrocardiogram, abnormal

electromyogram

encephalopathy

encephalopathy, progressive

exercise intolerance

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

familial

fatigue

fever

fluorescein angiography

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

granulomatosis with polyangiitis

granulomatous disease

heralding manifestation

high arched palate

Hirschprung's disease

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

intestinal pseudoobstruction

iris, abnormal

isoniazid

jaw pain

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

lactic acidemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukopenia

lymphoma involving CNS

lymphomatoid granulomatosis

MELAS syndrome

meningismus

meningoencephalopathy

mental retardation

methotrexate

methylhydrazine derivatives

migraine

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

movement disorder

MRI

MRI, abnormal

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myoclonus

myopathy

myopathy, centronuclear

myopathy, mitochondrial

nemaline rod myopathy

nerve conduction studies

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathy

neuropathy, peripheral

nystagmus, dissociated

nystagmus, vertical

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

orthostatic hypotension

Parkinsonism syndrome

percussion induced muscle contraction

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

POLG1 gene

polyneuropathy

pregnancy, neurologic complications in

procarbazine

prognosis

progressive neurologic disorder

ptosis, classification of

ptosis, familial

ptosis, unilateral

pulmonary infiltrates

sensorineural hearing loss

seronegative

short stature

skin, lesions in neurologic disorders

slit lamp examination

spasticity

spina bifida

splenomegaly

steroid therapy, CNS treatment and complications with

strokelike episodes

syringomyelia

systemic illness

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

thrombocytopenia

tinnitus

treatment of neurologic disorder

trinucleotide repeats

upgaze, paralysis of

vertigo

vinblastine

vincristine neurotoxicity

vocal cord paralysis

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Wildervanck's syndrome

wrist drop

Showing articles 1550 to 1600 of 1869 << Previous Next >>

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Pseudo-Horner's Syndrome
Arch Neurol 39:108-111, Thompson,B.M.,et al, 1982

Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982

The Neuropathology of Glycine Encephalopathy:Five Cases with Immunohistochemical & Ultrastructural Observations
Neurol 32:975-985, Agamanolis,D.P.,et al, 1982

Neuro-ophthalmic Signs & Symptoms of Hysteria
Neurol 32:757-762, Keane,J.R., 1982

Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982

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

Narcolepsy-Cataplexy
Arch Neurol 39:164-168, Kales,A.,et al, 1982

Periodic Meningitis & Familial Mediterranean Fever
Arch Int Med 142:378-379, Vilaseca,J.,et al, 1982

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

Where am I
BMJ 285:85-86, Godwin-Austen,R.B., 1982

Controlled Study of Metoprolol & Propranolol During Prolonged Administration in Patients with Essential Tremor
JNNP 45:893-897, Calzetti,S.,et al, 1982

Double-blind Controlled Study of Primidone in Essential Tremor:Preliminary Results
BMJ 285:608, Findley,L.J., 1982

Prevalence of Essential Tremor
Arch Neurol 39:750-751, Haerer,A.F.,et al, 1982

Genetics of Alzheimer's Disease
BMJ 284:1065-1066, Harris,R., 1982

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

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

A Surgical Approach To The Treatment Of Fetal Hydrocephalus
NEJM 306:1320-1325, Clewell,W.H.,et al, 1982

Motor Spastic Paraplegia & Unilateral Infra-nuclear Facial Palsy Complicating Tetanus
BMJ 285:477-478, Jain,M.K.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,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 Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

Essential Myoclonus
In Movement Disorder, CD Marsden & S Fahn (Ed) , Butterworth, London, 1982, p 207., , 1982

Benign Paroxysmal Torticollis in Infancy
Arch Dis Child 56:956-959, Deonna,T.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Neurological Aspects of Thyroid Dysfunction
Mayo Clin Proc 56:504-512, Swanson,J.W.,et al, 1981

Enhanced Ptosis in Myasthenia Gravis
Arch Neurol 38:531, Gorelick,P.B.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Familial Hemiplegic Migraine:EEG & CT Scan Study of Two Cases
Ann Neurol 10:392-295, Gastaut,J.L.,et al, 1981

Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
NEJM 305:955, Clewell,W.H.,et al, 1981

Primary Empty Sella & Rieger's Anomaly Of The Anterior Chamber Of The Eye
NEJM 304:90-93, Kleinmann,R.E.,et al, 1981

Twin Study of Parkinson Disease
Neurol 31:77-80, Duvoisin,R.C.,et al, 1981

Familial Recurrent Peripheral Facial Palsy
Arch Neurol 38:463-464, Auerbach,S.H.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

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

Dominant Inheritance of Intracranial Berry Aneurysm
BMJ 283:824-825, Evans,T.W.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

The Familial Nature of MS:Empiric Recurrence Risks for First, Second-, & Third-degree Relatives of Pts
Neurol 31:1039-1041, Sadovnick,A.D.,et al, 1981

Optic Neuritis in Familial MS
Neurol 31:1138-1142, Ebers,G.C.,et al, 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Intensive Evaluation of Referred Unclassified Neuropathies Yields Improved Diagnosis
Ann Neurol 10:222-226, Dyck,P.J.,et al, 1981

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

A Family Affected with Intestinal Polyposis & Gliomas
Ann Neurol 10:390-392, Todd,D.W.,et al, 1981

Showing articles 1550 to 1600 of 1869 << Previous Next >>