Neudle.com: myopathy congenital

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 750 to 800 of 2015 << Previous Next >>

Focal, Steroid Responsive Myositis Causing Dropped Head Syndrome
Muscle & Nerve 22:769-771, Biran,I.,et al, 1999

Incidental Findings on Brain Magnetic Resonance Imaging From 1000 Asymptomatic Volunteers
JAMA 282:36-39, Katzman,G.L.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Intravenous Immunoglobulin Treatment in Neurologic Disorders
Arch Neurol 56:1025-1027,1032, Sorensen,P.S., 1999

Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
Arch Neurol 56:1028-1032, Karussis,D.&Abramsky,O., 1999

Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

Maternal Thyroid Deficiency During Pregnancy and Subsequent Neuropsychological Development of the Child
NEJM 341:549-555,601, Haddow,J.E.,et al, 1999

Pediatric Third, Fourth, and Sixth Nerve Palsies:A Population-Based Study
Am J Ophthalmol 127:388-392, Holmes,J.M.,et al, 1999

Folic Acid for the Prevention of Neural Tube Defects
Pediartrics 104:325-327, Committee on Genetics, 1999

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

Aneurysms in Relatives of Patients with Subarachnoid Hemorrhage,Frequency and Risk Factors
Neurol 53:982-988, Raaymakers,T.W.M.&the MARS Study Group, 1999

Risks and Benefits of Screening for Intracranial Aneurysms in First-Degree Relatives of Patients with Sporadic Subarachnoid Hemorrhage
NEJM 341:1344-1350, The Magnetic Resonance Angiography in Relatives of, 1999

Initial Loss of Consciousness and Risk of Delayed Cerebral Ischemia After Aneurysmal Subarachnoid Hemorrhage
Stroke 30:2268-2271, Hop,J.W.,et al, 1999

A Sartorial Challenge
Lancet 354:996, Reading,P.J.,et al, 1999

MR Angiography with Three-Dimensional Time-of-Flight and Targeted Maximum-Intensity-Projection Reconstructions in the Follow-up of Intracranial Aneurysms Embolized with Guglielmi Detachable Coils
AJNR 20:1470-1475,1391, Kahara,V.J.,et al, 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

Fetal Surgery for Myelomeningocele, Promise, Progress, and Problems
JAMA 282:1873-1874,1819,1826, Simpson,J.L., 1999

Neural-Tube Defects
NEJM 341:1509-1519,1485, Botto,L.D.,et al, 1999

Antiepileptic Drug Regimens and Major Congenital Abnormalities in the Offspring
Ann Neurol 46:739-746, Samren,E.B.,et al, 1999

MR Angiography as a Screening Tool for Intracranial Aneurysms:Feasibility, Test Characteristics, and Interobserver Agreement
AJR 173:1469-1475, Raaymakers,T.W.M.,et al, 1999

Should We Screen for Familial Intracranial Aneurysm?
Stroke 30:312-316, Crawley,F.,et al, 1999

Treatment of Intracranial Aneurysms by Embolization with Coils,A Systematic Review
Stroke 30:470-476, Brilstra,E.H.,et al, 1999

Clinicopath Conf,Hepatitis C,Type II Cryoglobulinemia,Vasculitis,B-cell Lymphoma,Mononeuritis Multiplex,Case 3-1999
NEJM 340:300-307, , 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

The Clinical Spectrum of Sarcoglycanopathies
Neurol 52:176-179, Angelini,C.,et al, 1999

Validity of Prediction of the Site of Ruptured Intracranial Aneurysms with CT
Neurol 52:34-39, van der Jagt,M.,et al, 1999

Risk of Cerebral Angiography in Patients with Subarachnoid Hemorrhage,Cerebral Aneurysm,and Arteriovenous Malformation,A Meta-Analysis
Stroke 30:317-320, Cloft,H.J.,et al, 1999

Assessment of the Value of MR Imaging for Examining Patients with Angiographically Negative Subarachnoid Hemorrhage
AJR 172:201-206, Rogg,J.M.,et al, 1999

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Dyslexia
NEJM 338:307-312, Shaywitz,S.E., 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Unruptured Intracranial Aneurysms - Risk of Rupture and Risks of Surgical Intervention
NEJM 339:1725-1733,1774, The Internat'l Study of Unruptured Intracranial An, 1998

Risk of Recurrent Subarachnoid Hemorrhage After Complete Obliteration of Cerebral Aneurysms
Stroke 29:2511-2513, Tsutsumi,K.,et al, 1998

Terson Syndrome:CT Evaluation in 12 Patients
AJNR 19:743-747, Swallow,C.E.,et al, 1998

Small Retinal Hemorrhages as the Only Sign of an Intracranial Aneurysm
Am J Ophthalmol 125:401-403, Kiriakopoulos,E.T.,et al, 1998

Double-Blind Randomized Trial of Tramadol for the Treatment of the Pain of Diabetic Neuropathy
Neurol 50:1842-1846, Harati,Y.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Subarachnoid Hemorrhage:Aneurysm Detection ahnd Preoperative Evaluation with CT Angiography
Radiology 208:423-430, Velthuis,B.K.,et al, 1998

Imaging of the Peripheral Nervous System:Evaluation of Peripheral Neuropathy and Plexopathy
AJNR 19:1011-1023, Maravilla,K.R.&Bowen,B.C., 1998

Dilemma of Discontin of Anticoag Therapy for Pts with Intracran Hem & Mech Heart Valves
Neurosurg 42:769-773, Eelco,F.M.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
Neurol 51:1226-1227, Wasay,M.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Mild Traumatic Brain Injury,Toward Understanding Manifestations and Treatment
Arch Int Med 158:90-97, Kushner,D., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Showing articles 750 to 800 of 2015 << Previous Next >>