Neudle.com: muscle metabolic disorders of

Differential
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abdominal distention

abdominal muscle paralysis

abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, intracerebral

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acoustic nerve

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

activities of daily living scale

acute disseminated encephalomyelitis

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adenosine deaminase deficiency

advances in neurology

adverse drug reaction

Africa

agenesis of corpus callosum

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

aluminum

aminoacidopathies

aminoacidurias

aminoacylase 1 deficiency

amiodarone

amitriptyline

ammonia

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anterior horn cell disease

anterior tibial muscle weakness

anti DNA agent

antiarrhythmic drugs

antibiotics

antibiotics, neurologic complications with

antiphospholipid antibodies

aromatic amino acid decarboxylase deficiency

arthrogryposis multiplex

ascending paralysis

ascites

asparginase

aspartate aminotransferase

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

basophilic stippling of red blood cells

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

biotin deficiency, juvenile form

biotinidase deficiency

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

botulism immune globulin

brain biopsy, false negative

brain purpura

brainstem, dysfunction

burning feet, differential diagnosis of

burning paresthesia

burst suppression pattern, electroencephalogram

busulfan

cachexia

calcification, heart

calcification, intracranial

calcification, muscle

calcium oxalate crystals

calf hypertrophy

camptocormia

Canavan's disease

cancer, cerebrovascular accident complicating patients with

candida albicans

canned food

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carnitine deficiency myopathy

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, hyperattenuation

CAT scan, muscle

CAT scan, pelvis

cataracts

cataracts, congenital

central core disease

central nervous system, infection of

central pontine myelinolysis

cephalosporins

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral death, EEG in

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral ischemia

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

Chinese paralytic syndrome

chromosomal abnormality

chromosome 19

chromosome 20

chromosome 6

chronic fatigue syndrome

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

coma, classification of

coma, electroencephalography in

congestive heart failure

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical deafness

cortical hemorrhage

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

cytochrome c oxidase, deficiency

cytokines

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

developmental milestones

developmental milestones, loss of

developmental retardation

dialysis disequilibrium syndrome

diaphragmatic paralysis

diarrhea

diarrhea, bloody

diet

differential diagnosis

difficulty climbing stairs

dilantin

diphtheria

diplopia

disability, neurological

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

disulfiram

docetaxel

dopa responsive dystonia

down-beat nystagmus

downward deviation of eyes

drooling

dropped head syndrome

drought

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

drug overdose

dural sinus thrombosis

duvalumab

dysarthria

dysequilibrium syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

emergencies, neurologic

emtricitabine

encephalitis

encephalitis, autoimmune

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalomalacia

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, parainfectious

encephalopathy, progressive

enteritis

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

exercise-induced neurologic dysfunction

exome sequencing

eye movement, disorders of

eye, pain in

facial appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

feeding disorder

fever

fibrillations

fingernails, abnormal

frontal lobe, pathologic signs of

fucosidosis

fundus, abnormality of

fungal infection, CNS

gag reflex, depressed

gait disorder

galactorrhea

galactosemia

gammaglobulin therapy, intravenous

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycine

glycogen debranching enzyme deficiency

glycogen storage disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Gulf War syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

headache, sudden onset of

headache, vascular

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

heavy metal intoxication

hemianopia

hemianopia, transient

hemiballismus

hemiparesis

hemiparesis, transient

hemiplegia

hemoglobinuria

hemolytic-uremic syndrome

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus

herpes virus infection

histochemistry of muscle

hoarseness

homocysteine, serum

honey

human immunodeficiency virus type 1

hydrazine

hydrocephalus

hydroxychloroquine

hydroxyglutaric aciduria

hyperammonemic encephalopathy

hyperglycinemia, nonketotic

hypertensive encephalopathy

hypokalemic paralysis

hypoparathyroidism, idiopathic

hypophonia

hyporeflexia

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

immune checkpoint inhibitors

immune-related adverse events

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion body myositis

industrial neurologic disorders

infant, evaluation of

intellectual deterioration

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrathecal chemotherapy

intrinsic hand muscles, wasting of

ischemic exercise test

isoniazid

Jakob-Creutzfeldt disease

Kayser-Fleischer ring

Kearns-Sayre syndrome

keratoconjunctivitis

klippel feil syndrome

konzo

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

kyphosis

lacrimation

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

laminar necrosis, cortical

L-dopa

Leber's hereditary optic neuropathy

leg swelling

leg weakness, bilateral

leukemia, neurologic findings assoc.with

leukemia, prophylactic treatment of CNS

leukocyte enzyme abnormality

leukoencephalopathy, differential diagnosis

leukoencephalopathy, toxic

leukopenia

leukostasis

levamisole

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

limbic encephalitis

lipid storage disorder of CNS

lipid storage myopathy

lithium

liver disease

liver function enzymes

liver transplantation

lordosis

low back pain

Lowe's syndrome

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, lesion of

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphopenia

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malformation, CNS, congenital

malignant hyperpyrexia

manganese intoxication

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, chronic

meningitis, leukemic

meningoencephalopathy

mental retardation

mental status, abnormal

mental status, abnormal, acute

metabolic disorder, primary

metabolic disorder, primary-screening tests

metallic taste

methcathinone

methotrexate

methylglutaconic aciduria

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

metronidazole

microangiopathic hemolytic anemia

microangiopathy, brain

microcephaly

microinfarcts

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mild cognitive impairment

mimics

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gyral swelling

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, muscle

MRI, negative

MRI, paramagnetic effect

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

mucormycosis

multiple organ failure

multiple sclerosis

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle relaxant

muscle spasm

muscle stiffness

muscle strength, testing

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mussel poisoning

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenic crisis

myasthenic syndrome

myelitis, longitudinal

myeloneuropathy

myelopathy

myelopathy, tract-specific

myelopathy, vacuolar

myocarditis

myoclonic encephalopathy of infancy

myoclonus, stimulus sensitive

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, steroid induced

myopathy, thyroid disease causing

nemaline rod myopathy

neoplasm, hormone producing, ectopic

neoplasm, metastatic

neoplasm, metastatic to CNS

neoplasm, metastatic to lumbosacral plexus

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve conduction studies, sensory

neuraminidase deficiency

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuropathy, diphtheritic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, painful

neuropathy, peripheral

newborn, evaluation of

next-generation sequencing

numbness, generalized

nutritional deficiency

nystagmus

nystagmus, rotary

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular flutter

ocular motility, disorders of

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic chiasm, enlarged

optic nerve, enlarged

optic neuritis

optic neuropathy

organ transplantation

ornithine transcarbamylase deficiency

orthopnea

orthostatic hypotension

paralysis, acute areflexic

paraspinal muscle weakness

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

phosphorylase b kinase deficiency

pigmentary retinopathy

plasmapheresis

PLEDs

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poison, organophosphate

POLG1 gene

poliomyelitis

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

polyneuropathy, uremic

Pompe's disease of glycogen storage

Pompe's disease, infantile

pons, lesion of

porphyria

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

postpartum

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

procarbazine

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

propofol

proprioception, abnormal

proptosis

proteinuria

proximal muscle atrophy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pyramidal tract

pyramidal tract dysfunction

pyridoxine

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quadriplegia, transient

radiation therapy, CNS treatment and complications with

radiculitis

ragged-red fibers

rapidly progressing neurologic illness

rash

recurrent

recurrent laryngeal nerve paralysis

release phenomena

remote effect of cancer on the nervous system

renal failure

renal failure, acute

renal stones

renal transplantation

repetitive nerve stimulation

respirator

respiratory arrest

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retinal degeneration

retinopathy

retrovirus

reverse straight leg raising test

reversible neurologic disorder

salivation, excessive

scoliosis, neurologic association with

screening

second wind phenomena

sedation

sedimentation rate, elevated

seizure

seizure, children

seizure, drug-induced

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, treatment of

self harm

self-mutilation

selumetinib

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory level

sensory loss

sensory loss, glove-stocking

sensory symptoms

sensory testing

sensory testing, quantitative

serum lipase, elevated

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snake bite

snout reflex

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

speech disorder, childhood

speech, loss of

speech, unintelligible

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, metastasis to

spinal muscular atrophy

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

spontaneous remission

standing difficulty

staphylococcal protein A column therapy

status epilepticus, nonconvulsive

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

stooped posture

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subdural hematoma

suck, poor

suicide

sulfite oxidase deficiency

sulfone

superior sagittal sinus thrombosis

sweating

sweating, abnormality of

symmetric brain lesions

sympathomimetic drugs

syphilis, diagnosis and treatment

systemic illness

systemic lupus erythematosus

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

thrombotic microangiopathy

tone, muscle, increased

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transient neurologic deficit

transverse smile

treatment of neurologic disorder

tyrosine hydroxylase deficiency

tyrosinemia

uncal herniation

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uremic encephalopathy

urine test for metabolic disorders

urine test in toxic screen

urine, dark

vaccination, neurologic complications with

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

visual acuity, decreased

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weight loss

welder

Werdnig-Hoffman disease

Wernicke's encephalopathy

wheelchair

Whipple's disease

whistle, inability to

white matter disease

whole genome sequencing

x-linked mental retardation

Showing articles 150 to 200 of 18701 << Previous Next >>

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Positive Response to Edrophonium in Patients with Neurotoxic Envenoming by Cobras (NAJA NAJA PHILIPPINENIS)
NEJM 315:1444-1448, Watt,G.,et al, 1986

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Neurologic Complications of Carcinoid
Neurol 36:745-749, Parchell,R.A.&Posner,J.B., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Syndrome of Opsoclonus-Myoclonus in Hyperosmolar Nonketotic Coma
Ann Neurol 18:623-624, Matsumura,K.,et al, 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Diagnosis & Treatment of Lumbosacral Plexopathies in Patients with Cancer
Arch Neurol 41:1282-1285, Pettigrew,L.C.,et al, 1984

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984

The Neurotoxicity of Antibacterial Agents
Ann Int Med 101:92-104, Snavely,S.R.,et al, 1984

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Acute Generalized Polyneuropathy Accompanying Lithium Poisoning
Ann Neurol 6:360-362, Brust,J.C.M.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Dapsone Motor Neuropathy--An Axonal Disease
Neurol 26:514, Gutmann,L.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Treatment of Hydrazine-Induced Coma with Pyridoxine
NEJM 294:938, Kirklin,J.K.,et al, 1976

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Clinical Advances in the Evaluation of Deep Coma
MCV Quart 10:152, Suter,C., 1974

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Neurologic Disorders Seen In the Uremic Patient
Arch Int Med 126:781, Tyler,H.R., 1970

Neurologic Disorders in Renal Failure
Am J Med 44:734, Tyler,H.R., 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

A 35-Year-Old Man with Recurrent Asymmetric Lumbosacral and Cervical Plexopathy
Neurol 106:e214910, Tayade,K.S., et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

Showing articles 150 to 200 of 18701 << Previous Next >>