Neudle.com: congenital myopathy

Differential
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abdominal protrusion

acanthocytosis

acetazolamide

acid maltase deficiency

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome, medical precautions with

acquired immunodeficiency syndrome-related complex

acyl CoA dehydrogenase deficiency

adducted thumb

advances in neurology

adverse drug reaction

agenesis of corpus callosum

airway obstruction

alpha-fetoprotein

alveolar hypoventilation

amniocentesis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anesthesia, general

aneurysm, intracranial

ankle clonous

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

antiarrhythmic drugs

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, absorption

anticonvulsants, bioavailability

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, subtherapeutic

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

arthrogryposis multiplex

automatic implantable cardioverter-defibrillator

azidodeoxythymidine

bacterial infection

baldness

basal ganglia, calcification of

basal ganglia, infarction

Bassen-Kornzweig syndrome

benign congenital hypotonia

bulbar palsy, progressive

calcification, intracranial

calcium antagonist

calcium channel dysfunction

cataracts, congenital

Central America

central core disease

central nervous system, infection of

central nuclei, muscle

cerebral cortical atrophy

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

children

chloride channel dysfunction

cholelithiasis

chromosomal abnormality

chromosome 1

chromosome 5

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clinodactyly

clubfoot as related to neurologic disease

congenital birth defects

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

corpus callosum, thinning

cortical blindness

counselling

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delivery, complicated

dementia

developmental abnormality of brain

developmental disability

developmental milestones

developmental retardation

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin

disability, neurological

dislocated hip, congenital

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

dystrophin associated proteins

ear, abnormal

echocardiogram

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, induction

epidemic

epidemiology of neurology

episodic disorders

episodic neurologic deficits

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

familial hemiplegic migraine

fasciculation

fatigue

Fazio-Londe's disease

feeding disorder

fetal movements, reduced

genetic diagnosis, prenatal

genetic neurologic disorders

Guillain Barre syndrome

heavy metal intoxication

hemiparesis

hemorrhagic diathesis

highly active antiretroviral therapy

histochemistry

histochemistry of muscle

human immunodeficiency virus type 1

Huntington's chorea

Hurler's syndrome

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperkalemic periodic paralysis

hyperreflexia

hypertelorism

hypertrophic cardiomyopathy

hypokalemia

hypokalemic periodic paralysis

hypoxic encephalopathy

immunohistochemistry

immunomodulation

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

infection

intellectual deficit

intrauterine

intrauterine infection

intrauterine infection, viral

Kearns-Sayre syndrome

keratoconus

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

laminopathies

lamotrigine

Laurence-Moon-Bardet-Biedl syndrome

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

leukodystrophy

levonorgestrel

lid closure, weakness of

life expectancy

lissencephaly

liver function enzymes

LMNA gene

lordosis

macrocephaly

malformation, CNS, congenital

malignant hyperpyrexia

MELAS syndrome

Melkersson's syndrome

Miller-Dieker syndrome

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mucopolysaccharidoses

multicore myopathy

multiminicore disease

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle hypertrophy

muscle hypertrophy, congenital

muscle pain

muscle stiffness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

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, facioscapulohumeral

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, distal weakness

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, focal

myopathy, glycogen storage

myopathy, metabolic

myopathy, mitochondrial

myopathy, monomelic

myopathy, scleromyxedema

myopia

myositis

myositis ossificans, progressive

myotonia dystrophica, classification

myotonia, treatment of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

neoplasm, primary of CNS

nerve conduction studies

neuritis

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal migration disorder

neuropathy, peripheral

newborn, evaluation of

obstetric neurologic injuries

occipital lobe, infarction

occipital lobe, lesion of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

Oppenheim muscular dystrophy

opportunistic infection

oral contraceptives

orbicularis oculi muscle

pacemaker, cardiac-transvenous

paramyotonia congenita

paraparesis

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias

paroxysmal neurologic deficits

patient information and support

pectus excavatum

percussion induced muscle contraction

periodic paralysis

poison, mercury

poison, neurologic problems with

polydactyly

polyhydramnios

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymicrogyria

polymyositis

polymyositis, infantile

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

potassium channel antibodies

potassium channel dysfunction

practice guidelines

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

procainamide

progeria

prognosis

progressive muscular dystrophy

progressive neurologic disorder

pseudohypertrophy

pseudoretinitis pigmentosa

quadriparesis, progressive

quadriplegia, transient

quality of life

ragged-red fibers

rash

repetitive nerve stimulation

scoliosis, neurologic association with

screening

seizure

seizure, children

seizure, injury following

seizure, pregnancy

seizure, treatment of

seizure, treatment of, monotherapy

seizure, women

serum alanine aminotransferase

short stature

short thumb

skin, biopsy

skin, lesions in neurologic disorders

sloped shoulders

SMN1 gene

sodium channel dysfunction

South America

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 6

standing difficulty

stem cell transplantation

temporalis muscle wasting

term infant

tocainide

tongue, fasciculations of

transverse smile

trauma

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tubular aggregates, muscle

type 1 muscle fiber

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

visual fields, constricted

visual impairment

vital capacity

vitamin K

vitamin supplementation

vomiting, recurrent

Walker-Warburg syndrome

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

wheelchair

whistle, inability to

x-linked hydrocephalus

X-linked myopathy

Zika virus infection

Showing articles 900 to 950 of 2015 << Previous Next >>

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Aneurysmal Third-Nerve Palsies Presenting with Pleocytosis
Neurol 46:1176, Keane,J.R., 1996

Misdiagnosis of Symptomatic Cerebral Aneurysm Prevalence & Correlation with Outcome at Four Institutions
Stroke 27:1558-1563, Mayer,P.L.,et al, 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Intracranial Hemorrhage Associated with Cocaine Abuse:A Prospective Autopsy Study
Neurol 46:1291-1296, Nolte,K.B.,et al, 1996

Apolipoprotein E Genotyping in Alzheimer's Disease
Lancet 347:1091-1095, Tanzi,R.,et al, 1996

The Spectrum of Brain MR Abnormalities in Sickle-Cell Disease:A Report from the Cooperative Study of Sickle Cell Disease
AJNR 17:965-972, Moser,F.G.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Chronic Post-Traumatic Headache Often a Myth
Neurol 46:915-916, Warner,J.S.&Fenichel,G.M., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

MR Evaluation of Patients with Congenital Hyposmia or Anosmia
AJR 166:439-443, Yousem,D.M.,et al, 1996

Is Marfan Syndrome Associated with Symptomatic Intracranial Aneurysms?
Stroke 27:10-12, van den Berg,J.S.P.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Congenital Unilateral Facial Paralysis
Pediatrics 97:261-265, Shapiro,N.L.,et al, 1996

Dyslexia:A Hundred Years On
BMJ 313:1096-1097, Snowling,M., 1996

Basal Ganglia and Thalamic Infarction in Children
Arch Neurol 53:1252-1256, Brower,M.C.,et al, 1996

Cavernous Sinus Syndrome
Arch Neurol 53:967-971, Keane,J.R., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Neurologic Status of HIV-1 Infected Infants and Their Controls:A Prospective Study from Birth to 2 Yrs
Pediatrics 98:1109-1118, Belman,A.L.,et al, 1996

Cerebrovascular Complications of HIV in Children
AJNR 17:1913-1917, Shah,S.S.,et al, 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,et al, 1996

Moyamoya and Down Syndrome:Clinical and Radiological Features
Stroke 27:2131-2135, Cramer,S.C.,et al, 1996

Peripheral Neuropathy Secondary to Docetaxel (Taxotere)
Neurol 46:108-111, 21996., New,P.Z.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

White Matter MR Hyperintensities in Adult Patients with Congenital Rubella
AJNR 17:99-103, Barton Lane,E.,et al, 1996

Visual Loss after Neurosurgical Repair of Paraclinoid Aneurysms
Ophthalmol 102:905-910, Rizzo,J.F.,III, 1995

Folate Levels and Neural Tube Defects:Implications for Prevention
JAMA 274:1698-1702, 17171995., Daly,L.E.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Detection and Assessment of Intracranial Aneurysms:Value of CT Angiography with Shaded Surface Display
AJR 165:1497-1502, Liang,E.Y.,et al, 1995

Showing articles 900 to 950 of 2015 << Previous Next >>