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 1800 to 1850 of 1869 << Previous Next >>

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Scalloped Pupils in Familial Amyloidosis
NEJM 293:914, Lessell,S.,et al, 1975

Unrecognized Adult Phenylketonuria
NEJM 289:395, 1973, 289:1040, 1973, 290:1084., Perry,T.,et al, 1974

Ptosis-Toxiocology of the Eye
p 814, , 1974

Efficacy of Chronic Propranolol Therapy in Action Tremors of the Familial, Senile or Essential Varieties
NEJM 290:984, Winkler,G.,et al, 1974

Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57
1974., , 1974

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Specific Laboratory Test for Diagnosis of MS
BMJ 1:412, Field,E.J.,et al, 1974

Vincristine Neurotoxicity
Ann Int Med 80:733-737, Rosenthal,S.,et al, 1974

Treatment of Essential Tremor with Propranolol
Lancet 205, Jan1973., , 1973

Tay-Sachs Disease-The Use of Tears for the Detection of Heterozygotes
NEJM 289:1072, Carmody,P.,et al, 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Niemann-Pick Disease
Correspondence NEJM 289:590, Dacremont,G.,et al, 1973

Infantile Metachromatic Leukodystrophy
NEJM 288:1365, 14051973., Leroy,J.,et al, 1973

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

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Narcolepsy
NEJM 288:1156, Zarcone,V., 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

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

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

Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973

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

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

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

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

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

Dysautonomia, Its Significance in Neurologic Disease (Specialty Conference)
Calif Med 117:28, Wichser,J.,et al, 1972

Differential Diagnosis of Tremors
Med Clin North Am 56:1363, Fahn,S., 1972

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

Neurosyphilis
JAMA 219:726, Hooshmand,H.,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

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

Familial Calcification of the Basal Ganglions A Metabolic & Genetic Study
NEJM 285:72, Moskowitz,M.,et al, 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

"Steroid-induced"Mydriasis & Ptosis
Investig Ophthalmol Jun 1971, p 424., Newsome,D.,et al, 1971

Neurocutaneous Disease
in Dermatology in General Medicine, Fitzpatrick, et al, eds, McGraw Hill, 1971, pp. 1379-1434., Adams,R., 1971

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

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

Whipple's Disease & Papilledema
Arch Int Med 123:74, Switz,D.M.,et al, 1969

Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
Am J Ophthalmol 67:561, Johnson,R.V.,et al, 1969

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

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

Showing articles 1800 to 1850 of 1869 << Previous Next >>