Neudle.com: abnormal neuromuscular junction

Differential
(Click to cross reference)

accomodation, abnormal

acetylcholine receptor

acetylcholine receptor antibody

acute intermittant porphyria

adverse drug reaction

agammaglobulinemia

ageusia

algorithm

alveolar hypoventilation

aminoglycoside

aminopyridine, 4

amphiphysin antibodies

ampicillin

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, myasthenic syndrome with

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticholinergic drugs, side effects of

anticholinesterase

anticonvulsants

anticonvulsants, untoward effects of

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

azathioprine

barium poisoning

beta adrenergic blocker

Bielschowsky head tilt test

botulinum toxin

botulinum toxin, complications of

botulism

botulism antitoxin

botulism immune globulin

calcium antagonist, side effects of

cancer associated myopathy

cerebellar degeneration

cerebellar lesion

cerebellum

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

chemical weapons

chemotherapy, CNS treatment and complications with

children

Chinese paralytic syndrome

chloroquine

chlorpromazine

chronic progressive external ophthalmoplegia

ciguatera poisoning

ciprofloxacin

citrate

Clinical Pathologic Conference(C.P.C.)

cocaine

collapsin response mediator protein 5 IgG

coma

comorbidities

complications

congenital myasthenic syndromes

constipation

contactin associated protein like 2 antibodies

contrast agents, neurotoxicity of

conversion reaction

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

demyelinating disease

dermatomyositis

descending paralysis

developmental retardation

diaphragmatic paralysis

drug abuse, neurologic complications of

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram

electromyogram

electromyogram, decremental response

electromyogram, incremental response

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

encephalopathy

encephalopathy, septic

epidemiology of neurology

erythromycin

exercise

eye movement, disorders of

face, numbness of

facial nerve palsy

facial weakness

facial weakness, bilateral

gag reflex, depressed

gait disorder

gammaglobulin therapy, intravenous

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

gene mutation

genetic neurologic disorders

genetic testing

Graves ophthalmopathy

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

head bobbing

headache

heat intolerance

heavy metal intoxication

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

iatrogenic neurologic disorders

ileus, paralytic

immune checkpoint inhibitors

immune-related adverse events

immunologic disease

immunology and the nervous system

immunosuppressive agents

immunotherapy

impotence

inappropriate antidiuretic(A.D.H.)hormone

infant, evaluation of

insect sting

insecticides

interferon

internuclear ophthalmoplegia

Kearns-Sayre syndrome

leg weakness, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

levonorgestrel

lid abnormalities

lid closure, weakness of

lid twitch

life support, withdrawal of

life sustaining treatment

limbic encephalitis

lipoprotein receptor-related protein 4

lithium

liver transplantation

magnesium salts

malignancy screen

malignancy, occult

medical-legal aspects of neurology

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

muscle atrophy, static

muscle strength, testing

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

MuSK antibodies

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, cold test for

myasthenia gravis, congenital

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, drug induced

myasthenia gravis, etiology of

myasthenia gravis, exacerbation

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, paraneoplastic

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, receptor site in

myasthenia gravis, sensory loss with

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenia gravis, unmasked

myasthenia gravis, variants

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

myocarditis

myopathy

myopathy, acute

myopathy, critically ill

myopathy, drug-induced

myopathy, mitochondrial

myopathy, necrotizing

myopathy, steroid induced

nerve conduction studies

neuroendocrinology

neuroleptic

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic history

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuronal cell surface antigen

neuronopathy, sensory

neuroophthalmology

neuropathy

neuropathy, acute

neuropathy, diphtheritic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, paraneoplastic

neuropathy, peripheral

ocular motility, disorders of

oculovestibular reflex

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, total

opsoclonus

opsoclonus-myoclonus syndrome

optic neuritis

oral contraceptives

orbicularis oculi muscle

organ transplantation

paraneoplastic cerebellar degeneration

peripheral nerve, lesion of

phenothiazine

plasmapheresis

plasmapheresis, complications of

pleocytosis of cerebrospinal fluid

POEMS syndrome

poison, neurologic problems with

poison, organophosphate

polymerase chain reaction

polymyositis

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

porphyria

postoperative neurologic complications

practice guidelines

pregnancy, neurologic complications in

progressive neurologic disorder

propranolol

prostigmine

pseudointernuclear ophthalmoplegia

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

remote effect of cancer on the nervous system

renal failure

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory paralysis, pharmacologic

retinopathy

review article

rheumatoid arthritis, neurologic complications of

rhinorrhea

rituximab

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

single-fiber electromyography

sleep

sleep apnea

snake bite

spinal cord, injury of

standing difficulty

status asthmaticus

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage, prognosis

suck, poor

suicide

superior oblique myokymia

superior oblique palsy

systemic lupus erythematosus

tensilon test, false positive

thymus and neuromuscular function

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

tracheostomy

treatment of neurologic disorder

trochlear nerve palsy

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weaning from respirator, failure to

weight loss

Wernicke's encephalopathy

wheelchair

workup

xerostomia

Showing articles 700 to 750 of 15030 << Previous Next >>

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Late Complication of Undetected Odontoid Fracture in Children
BMJ 300:319-320, Alp,M.S.&Crockard,H.A., 1990

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Ataxic Sensory Neuropathy and Dorsal Root Ganglionitis Associated with Sjogren's Syndrome
Ann Neurol 27:304-315, Griffin,J.W.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Periventricular Involvement in CNS Lymphomatoid Granulomatosis:MR Demonstration
J Comput Assist Tomogr 14:291-293, Smith,A.S.,et al, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Kearns-Sayre Syndrome and Dilated Cardiomyopathy
Neurol 40:553-554, Tveskov,C.&Angelo-Nielsen,K., 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Central Lesions in Chronic Inflammatory Demyelinating Polyneuropathy:An MRI Study
Neurol 40:476-478, Feasby,T.E.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Aggravation of Human and Experimental Myasthenia Gravis by Contrast Media
Neurol 40:1623-1625, Eliashiv,S.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Chronic Neurologic Manifestations of Lyme Disease
NEJM 323:1438-1444, Logigian,E.L.,et al, 1990

Involvement of the CNS in Chronic Inflammatory Demyelinating Polyneuropathy:A Clinical Electrophys & MRI Study
JNNP 53:789-793, Ormerod,I.E.C.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Heart Disease is Myasthenia Gravis
Tidsskr Nor Laegeforen 110:1209-1211, Mygland,A.,et al, 1990

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
Ann Neurol 26:583-587, Vista,G.,et al, 1989

Duchenne Muscular Dystrophy Carrieris
Neuroradiology 31:373-376, Matsumura,K., 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Spectrum of Neurologic Events Following Cardiac Transplantation
Stroke 20:1586-1589, Sila,C.A., 1989

Chiari Type I Malformation in Children
J Pediatr 115:573-576, Dure,L.S.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Chronic Myelopathies Associated with HTLV-I, A Clinical, Serologic, and Immunovirologic Study of 10 Patients in France
Arch Neurol 46:255-260, Gout,O.,et al, 1989

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Medical Problems of Musicians
NEJM 320:221-227, 246-2481989., Lockwood,A.H., 1989

Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
Neurol 39:244-248, Horoupian,D.S., 1989

Brain-Stem Auditory Evoked Potential Abnormalities with Unilateral Brain-Stem Lesions Demonstrated by MRI
Arch Neurol 46:295-299, Markand,O.N.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Ocular Pseudomyasthenia or Ocular Myasthenia'Plus':A Warning to Clinicians
Neurol 39:1150-1154, Moorthy,G.,et al, 1989

Electrophysiological and MRI Evaluation of Neurological Involvement in Behcet's Disease
JNNP 52:749-754, Besana,C.,et al, 1989

Neurobrucellosis:Clinical Characteristics, Diagnosis, and Outcome
Neurol 39:498-501, AlDeeb,S.M.,et al, 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Showing articles 700 to 750 of 15030 << Previous Next >>