Neudle.com: X linked myopathy

Differential
(Click to cross reference)

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 550 to 600 of 1544 << Previous Next >>

Microscopic Polyangiitis: Clinical and Laboratory Findings in Eighty-five Patients
Arthritis Rheum 42:421--430, Guillevin, L.,et al, 1999

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

The Management of Minor Closed Head Injury in Children
Pediatrics 104:1407-1415, Cmte on Quality Improvement,American Academy of Pe, 1999

Difficult Asthma or Churg-Strauss Syndrome? Steroids May be Masking Undiagnosed Cases of Churg-Strauss Syndrome
BMJ 318:475-476, D'Cruz,D.P.,et al, 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

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

Late-Onset Myasthenia Graivs,A Changing Scene
Arch Neurol 56:25-27, Aarli,J.A., 1999

Outbreak of Nipah-Virus Infection Among Abattoir Workers in Singapore
Lancet 354:1253-1256,1222, Paton,N.I.,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

Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
Muscle & Nerve 22:1479-1497, Dalakas,M.C., 1999

Clinicopath Conf:Carcinoma of Stomach with Leptomeningeal Carcinomatosis, DIC, Cortico-subcortical Infarcts
NEJM 340:1099-1106, Case 10-1999, 1999

Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Critical Illness Neuropathy and Myopathy
Arch Neurol 56:527-528, Gutmann,L.&Gutmann,L., 1999

Clinicopath Conf:Burkitt-Like B-Cell Lymphoma, Nocardiosis
NEJM 340:1188-1196, Case 11-1999, 1999

Significance of Vomiting After Head Injury
JNNP 66:470-473, Nee,P.A.,et al, 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999

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

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

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

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

MRI of Arachnoid Granulations Within the Dural Sinuses Using a FLAIR Pulse Sequence
British Jour Radiol 72:1046-1051, Ikushima,I.,et al, 1999

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

Air Bag-Related Deaths and Serious Injuries in Children:Injury Patterns and Imaging Findings
AJNR 19:1599-1607,1591, Marshall,K.W.,et al, 1998

Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
Neurol 51:1039-1045, Seale,C.G.,et al, 1998

Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
Neurol 51:944-948, Rpt of the Quality Stnds Subcmte AAN, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 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

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

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

A Population-Based Study of Seizures after Traumatic Brain Injuries
NEJM 338:20-24, Annegers,J.F.,et al, 1998

Lovastatin for X-Linked Adrenoleukodystrophy
NEJM 339:702-703, Singh,I.,et al, 1998

Acute Myopathy After Liver Transplantation
Neurol 50:46-53, Campellone,J.V.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Sporadic Incusion-Body Myositis and hereditary Inclusion-Body Myopathies
Arch Neurol 55:915-920, Askanas,V.&Engel,W.K., 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Showing articles 550 to 600 of 1544 << Previous Next >>