Neudle.com: X linked myopathy

Differential
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abdominal tenderness

abducens nerve paralysis

abducens nerve paralysis, bilateral

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

angiotensin-converting enzyme

anorexia

antibiotics

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

anti-myeloperoxidase

antineutrophil cytoplasmic autoantibodies

aortic valve, insufficiency

aphasia

arachnoiditis

arcuate scotoma, differential diagnosis of

aspartate aminotransferase

ataxia telangiectasia

atrioventricular block

attention deficit disorder with hyperactivity

autism

autoimmune disease

autonomic dysfunction

Babinski sign

bacterial endocarditis, neurologic manifestations of

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

Beau's lines

bitemporal visual field defect

blindness

blood cultures

bone marrow suppression

bone marrow transplantation

brain atrophy

brain biopsy

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, tuberculoma of

calcification, intracranial

calcification, muscle

calf hypertrophy

carcinoma

carcinoma of lung

carcinoma of pancreas

cardiomegaly

cardiomyopathy

cardiovascular disease

cauda equina, lesion of

central nervous system, infection of

central nuclei, muscle

cerebellar ataxia, children

cerebellum, disease of

cerebellum, neoplasms of

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, multiple

cervical spine

cervical spine abnormality

chest pain

chest x-ray, abnormal

chromosomal abnormality

chromosome 14

Churg-Strauss syndrome

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

Cogan's syndrome

cognition

collagen vascular disease

congestive heart failure

conjunctival injection

conjunctivitis

contractures, joint

coronavirus

corpus callosum, lesion of

corpus callosum, thinning

cortical infarction

cough

COVID-19

cranial nerve palsies

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

degenerative diseases of CNS

delirium

dementia

dementia, childhood

demyelinating disease

depression

dermatitis

dermatomyositis

dermatomyositis, childhood

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

diet

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin

dilantin, hypersensitivity to

diplopia

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

diurnal variation

DNA probes

dopa responsive dystonia

drug induced neurologic disorders

dysarthria

dysarthria-clumsy hand syndrome

dystonia, etiology of

dystonia, painful

dystrophic calcification

dystrophin

ear, abnormal

echocardiogram

echocardiogram, transesophageal

echocardiogram, transthoracic, false negative

edema, pedal

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electronystagmography

electroretinograph

embolism, septic

Emery-Dreifuss muscular dystrophy

endocarditis, acute bacterial

endocarditis, infectious

endophthalmitis

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

eye movement, disorders of

eye, pain in

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

fatty acid, elevated plasma content

ferritin, elevated

fetus

fever

fingernails, abnormal

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

fundus, abnormality of

gait disorder

gallium scan

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal bleeding

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gowers maneuver

granuloma, eosinophilic

granulomatosis, allergic

granulomatous disease

granulomatous hypophysitis

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

gynecomastia

Hallervorden Spatz disease

hallucination

hallucination, auditory

hallucination, visual

hand weakness

Hand-Schuller-Christian disease

headache

headache, bifrontal

headache, positional

headache, progressive

heavy metal intoxication

heliotrope rash

hemangioblastoma

hematuria, microscopic

hemianopia, homonymous

histochemistry of muscle

hormone replacement

Huntington's chorea

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperadrenalism

hyperamylasemia

hypercalcemia

hypereosinophilic syndrome(HES)

hyperesthesia

hypergammaglobulinemia

hypersensitivity reaction

hypersomnia

hypertension

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypogonadism

hypokalemic periodic paralysis

hypokinetic left ventricle

hypothalamus, disturbance of

iatrogenic neurologic disorders

imbalance

immunodeficiency

immunohistochemistry

immunosuppressive agents

impulsivity

inclusion body myositis

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

Kearns-Sayre syndrome

keratitis

lacrimation

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

leg spasms

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

level of consciousness, decreased

life expectancy

livedo reticularis

liver disease

liver function enzymes

lymphadenopathy, hilar

lymphocyte capping, diminished

lymphoid adenohypophysitis

malignant hyperpyrexia

masked facies

mastoiditis

mediastinum, mass of

medulla oblongata, lesion of

Mees lines

memory, impairment of

meningitis, recurrent

meningoencephalitis

meningomyelitis

mental retardation

mental retardation, familial

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

misdiagnosis

mitral valve lesion

mitral valve vegetation

molecular genetics

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, muscle

MRI, sulcal hyperintensity

mucopolysaccharidoses

multiple sclerosis, misdiagnosis

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, receptor site in

myelitis, longitudinal

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myxedema, neurologic manifestations of

nasal polyp

nasal septum, perforation of

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

neuritis, heavy metals causing

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuronopathy

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, toxic

neuropathy, vasculitic, systemic

obsessive-compulsive disorder

ocular myopathy

odynophagia

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, total

optic atrophy

optic nerve

optic neuropathy

orange peel appearance of skin

otitis, neurologic complications with

Parkinsonism syndrome

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peroxisomal disease

pheochromocytoma

photophobia

pigmentary retinopathy

pituitary, enlargement

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polymyositis, eosinophilic

polyneuropathy

pons, lesion of

position sensation, abnormal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

proteinuria

prothrombin time, prolonged

proximal muscle atrophy

psychiatric problems in neurologic disorders

pulmonary infiltrates

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal artery occlusion

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rhinorrhea

rickettsial organism

rigid spine syndrome

rippling muscle disease

risk factors

Rocky Mountain spotted fever

sarcoidosis

sarcoidosis, CNS

scleroderma

scleroderma, neurologic involvement with

scoliosis

scotoma

sedimentation rate

sedimentation rate, elevated

seizure

seizure, familial

sella turcica, enlargement of

sensorineural hearing loss

serologic testing

serum alanine aminotransferase

serum sickness

severe acute respiratory syndrome

skin, lesions in neurologic disorders

skin, tight

skull x-ray

skull x-ray, abnormal

sonophobia

southeast asia

Southern immunoblot test

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinocerebellar degeneration

steroid therapy, CNS treatment and complications with

Stevens-Johnson syndrome

streptococcus pneumoniae

subarachnoid hemorrhage

subcutaneous edema

suprasellar lesion

sweating

sweating, abnormality of

swimming

systemic illness

systemic lupus erythematosus, drug induced

tachycardia

tandem gait, ataxic

tapetoretinal degeneration

telangiectases

telangiectases, periungual

testicular atrophy

testicular biopsy

testicular enlargement

tongue, fasciculations of

tonsillar herniation of cerebellum

toxic encephalopathy

toxic oil syndrome

transient ischemic attack

travel, foreign

treatment of neurologic disorder

tremor

tremor, intention

tremor, postural

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

tuberculosis, miliary

tumor necrosis factor inhibitor

uncal herniation

uremia

urine test in toxic screen

Usher's syndrome

uveitis

vasculitides

Venereal Disease Research Laboratory test

vertigo

very long chain fatty acids

viral myopathy

vision, blurred

visual acuity, decreased, monocular

visual field defect

visual loss

visual loss, sudden-unilateral

vital capacity

Von Hippel Lindau

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weakness, proximal

web sites

weight loss

Western immunoblot test

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

X-linked myopathy

x-linked myopathy with excessive autophagy

x-ray, cervical spine

Showing articles 650 to 700 of 1544 << Previous Next >>

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Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
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Clinicopath Conf
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Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Acute Demyelinating Polyneuropathy with Arsenic Ingestion
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Inclusion Body Myositis:Clinical and Pathological Boundaries
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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
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Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
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Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
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Diagnosing Motor Neurone Disease
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AAEM Case Report#13:Diabetic Amyotrophy
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Critical Illness Myopathy and Neuropathy
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Motor Neuropathy Due to Docetaxel and Paclitaxel
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Intelligence and the X Chromosome
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X-Linked Malformation of Neuronal Migration
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
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Clinical Heterogeneity of Adhalin Deficiency
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Apolipoprotein E Genotyping in Alzheimer's Disease
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Pure Motor Hand Weakness
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Chronic Post-Traumatic Headache Often a Myth
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Adult-Onset MELAS
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Showing articles 650 to 700 of 1544 << Previous Next >>