Neudle.com: hand contractures

Differential
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accommodation

accomodation, abnormal

advances in neurology

adverse drug reaction

anterior tibial muscle weakness

arthrogryposis multiplex

atrioventricular block

attention deficit disorder with hyperactivity

autoantibodies

autoimmune disease

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

biopterin deficiency

blinking

blinking, reduced

bone marrow transplantation

Brown-Vialetto-Van Laere syndrome

burning paresthesia

cachexia

calcification, intracranial

cardiovascular disease

caries

carpal tunnel syndrome

cerebellar atrophy, primary

cerebral cortical atrophy

cerebral embolism

cerebral embolism, carotid origin

cerebral palsy

cerebrospinal fluid, abnormal

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical spine

cervical spine abnormality

chromosomal abnormality

chromosome 14

chromosome 17

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition

cogwheel rigidty

congenital infection, CNS

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

consanguinity

contractures, joint

contrast agents, neurotoxicity of

convergence

convergence, impaired

cornea, opacity of

corpus callosum, lesion of

cough

cranial neuropathy

cranial neuropathy, multiple

crawl regression

C-reactive protein, elevated

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cry, weak

cryptorchidism

cytomegalovirus infection

cytomegalovirus infection, congenital

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

dialysis

diamond on quadriceps

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability rating scale, neurological

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

drooling

drug induced neurologic disorders

dystonia, treatment of

dystrophic calcification

dystrophin

electrocardiogram, abnormal

electromyogram

Emery-Dreifuss muscular dystrophy

encephalopathy

encephalopathy, progressive

endemic area

enzyme, defect

enzyme, muscle disease

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

epileptic encephalopathy

facial appearance, abnormal

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

gamma amino butyric acid

genetic neurologic disorders

genetic testing

glabellar sign

glutamic acid decarboxylase, antibody

Guillain Barre syndrome

heart block, complete

heart murmur

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

histochemistry of muscle

hyperpigmentation of skin

iatrogenic neurologic disorders

imbalance

immunosuppressive agents

implantable cardioverter defibrillator

inclusion body myositis

intellectual deterioration

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

jaw contractures

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lateral cutaneous nerve of forearm

liver function enzymes

liver transplantation

lordosis

L-tryptophan

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lysosomal storage disease

malignant hyperpyrexia

marche a petits pas

masked facies

median neuropathy

meningitis, CSF cell count-normal

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal antibodies

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, complications with

MRI, contraindications

MRI, contrast enhanced

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle strength, testing

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, familial incidence of

myopathy, hypocalcemic

myopathy, quadriceps

myositis

myositis, acute of childhood

myositis, post infectious

nephrogenic systemic fibrosis

nerve conduction studies

nerve enlargement

nerve hypertrophy

nerve injury

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuropathology

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, peripheral

orange peel appearance of skin

overlap syndrome

pacemaker, cardiac-transvenous

pain

pain, calf

pain, leg

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinsonism syndrome

periventricular leukomalacia

personality change

pes cavus

phlebotomy

photosensitivity, skin

pigmentary retinopathy

pneumonia

polymerase chain reaction

polymyalgia rheumatica

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

prolactin, elevated

proximal muscle atrophy

pruritus

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pyramidal tract dysfunction

rash

Red flags

reflex sympathetic dystrophy

renal failure

renal tubular acidosis

repetitive nerve stimulation

riboflavin transporter deficiency

rickets

rigid spine syndrome

rigidity

rippling muscle disease

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

sensorineural hearing loss

skin, lesions in neurologic disorders

speech disorder, childhood

steroid therapy, CNS treatment and complications with

systemic juvenile idiopathic arthritis

treatment of neurologic disorder

tyrosine hydroxylase deficiency

urea-cycle enzymopathies

uremia

urine test for metabolic disorders

voice, abnormality of

Walker-Warburg syndrome

walking

walking frame

walking, delayed

walking, difficulty with

weakness

weakness, congenital

weakness, generalized

weakness, progressive

x-ray, cervical spine

Showing articles 750 to 800 of 844 << Previous Next >>

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Amyloid Neuropathy & Tremor in Waldenstrom's Macroglobulinemia
Arch Neurol 37:240-242, Bajada,S.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Interaction of Lithium & Phenytoin
BMJ 1:610-611, MacCallu,W.A., 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
Ann Neurol 8:329-332, Zifkin,B.,et al, 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Giant Axonal Neuropathy
Arch Neurol 36:107-108, Mizuno,Y.,et al, 1979

Upper Trunk Brachial Plexopathy in Football Players
JAMA 241:1480-1482, Robertson,W.C.,et al, 1979

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Acute Generalized Polyneuropathy Accompanying Lithium Poisoning
Ann Neurol 6:360-362, Brust,J.C.M.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Valproic Acid, Review of a New Antiepileptic Drug
Arch Neurol 36:393-398, Bruni,J.,et al, 1979

Tremor Due to Sodium Valproate
Neurol 29:1177-1180, Hyman,N.M.,et al, 1979

Clinical Pathological Conference, Peripheral Neuropathy in Leprosy
NEJM 300:546-553, Dawson,D., 1979

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Propranolol for Severe Post-head Injury Action Tremor
Neurol 28:197, Ellison,P.H., 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Chlordecone Intoxication in Man
Neurol 28:626, Taylor,J.R.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Peripheral Nerve Conduction in Patients with a Cervical Rib & Band
Ann Neurol 4:124-129, Gilliatt,R.W.,et al, 1978

Tricyclic Antidepressants
NEJM 299:1106-1109, 1168-11721978., Hollister,L., 1978

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

The Serological Diagnosis of St. Louis Encephalitis in Patient with Syndr. of Opsoclonia, Body Tremulousness, & Benign Encephalitis
Ann Neurol 1:596, Estrin,W., 1977

Hangman's Fracture Subsequent to Shaking in an Infant
Ann Neurol 2:82, McGrory,B.E., 1977

Radicular Compression in Multifocal Eosinophilic Granuloma
Arch Neurol 34:786, Eil,C.,et al, 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Familial Essential Myoclonus
Brain 93:131-138, Korten,J.J.,et al, 1977

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Dapsone Motor Neuropathy--An Axonal Disease
Neurol 26:514, Gutmann,L.,et al, 1976

Anticonvulsant-induced Dyskinesias:A Comparison with Dyskinesias Induced by Neuroleptics
JNNP 39:1210, Chadwick,D.,et al, 1976

Dystonia & Choreoathetosis in Multiple Sclerosis
Arch Neurol 33:590, Bachman,D.S.,et al, 1976

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Drug Therapy of Parkinsonism
NEJM 295:814, Bianchine,J.R., 1976

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Showing articles 750 to 800 of 844 << Previous Next >>