Neudle.com: cobalamin deficiency

Differential
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abdominal distention

aciduria

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

Addison's disease

adverse drug reaction

affective disorders

agitation

alcohol

alcoholic polyneuropathy

amyloid angiopathy, cerebral

anemia

anemia, hemolytic

anemia, iron deficiency

anemia, megaloblastic

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

ankle edema

anorexia

anticonvulsants, untoward effects of

antiendomysial antibodies

areflexia

arsenic

arterial dissection, precipitating events

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

B 12 deficiency, infants

B 12 metabolism, defective

B12

B12 binding protein, abnormal

Babinski sign

bacterial infection

basal ganglia, lesion of

blood dyscrasias, neurologic findings with

burning feet, differential diagnosis of

burning hands

burning paresthesia

carbon monoxide poisoning

carcinoma of pancreas

carotid artery disease

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, dementia

CAT scan, emission, abnormal

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral infarction

cerebral ischemia

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, prevention of

cerebrovascular disease, risk factors in

cervical spine

cervical spine injury

cervical spondylosis

chemotherapy, CNS treatment and complications with

Clinical Pathologic Conference(C.P.C.)

clonus

clubbing of fingers

cobalamin C deficiency

cognition

colchicine

collagen vascular disease

coma

complications

concentration, impaired

confusion

congestive heart failure

controversies in neurology

copper deficiency

corpus callosum

corpus callosum, lesion of

cortical blindness

C-reactive protein, elevated

Cushing's syndrome

delusion

dementia

dementia, clinical diagnosis

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

depression

developmental milestones, loss of

developmental retardation

differential diagnosis

dilantin

dilantin, toxicity

disability, neurological

dissociated sensory loss

distal muscle weakness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy

encephalopathy, Hashimoto's

epidemiology of neurology

ergotism

evidence-based research

fine motor function, impaired

folic acid

folic acid deficiency

gastrectomy, neurologic complications following

gastrointestinal disease, neurologic complications

gene mutation

genetic neurologic disorders

glucose tolerance test, abnormal

hallucination, auditory

hemorrhagic diathesis

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

hip flexor weakness

Hispanics

histamine-2 receptor blockers

HLA

homocysteine, serum

homocystinuria

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

hyperpigmentation of skin

hyperreflexia

hypersegmented polys

hypertensive encephalopathy

hypopigmentation of skin

iatrogenic neurologic disorders

imbalance

inappropriate behavior

inattention

inborn errors of metabolism

incontinence, fecal

incoordination

infant, evaluation of

infantile tremor syndrome

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intestinal biopsy

intracerebral hemorrhage

laboratory values, normal

lactic dehydrogenase(LDH)

laughing, pathologic

leg numbness

leg weakness, bilateral

lethargy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lhermitte's sign

limb shaking

limbic encephalitis

liver function enzymes

long bone lesion

low back pain

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

malabsorption

malabsorption syndrome

memory, defect of recent

memory, impairment of

meningitis

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metformin

methylmalonic acid, serum

methylmalonic acidemia

midbrain, lesion of

migraine

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

monoclonal gammopathy

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

muscle weakness

myasthenia gravis

myelitis, longitudinal

myeloma, osteosclerotic

myeloneuropathy

myelopathy

myelopathy, tract-specific

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neural tube defect

neuritis

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neuropathy, etiologies of

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, work up for

neuropsychiatry

neurotoxic

neurotoxin

newborn, evaluation of

numbness, generalized

nutritional deficiency

nystagmus

obesity

old age, neurology of

optic atrophy

optic neuritis

optic neuritis, etiology of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, nutritional

organomegaly

orthostatic hypotension

paresthesias, generalized

paresthesias, hands

Parkinson disease

pellagra

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

personality change

phenothiazine, dyskinesia associated with

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

plasma R binder deficiency

plasmacytoma

POEMS syndrome

polyneuropathy

polyradiculoneuropathy

porphyria

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

posterior tibial nerve

posterior tibial nerve compression

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

proton pump inhibitors

pseudoathetosis

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

quadriparesis

radiation therapy, CNS treatment and complications with

Red flags

regional enteritis

remote effect of cancer on the nervous system

renal failure

retinal hemorrhages

reversible neurologic disorder

sensory loss, cutaneous

sensory loss, glove-stocking

skin, lesions in neurologic disorders

somatosensory evoked potentials

spasticity

speech, pressured

spinal cord

spinal cord, cervical

spinal cord, lesion of

symmetric brain lesions

syncope

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tachycardia

tangential

tarsal tunnel syndrome

thyroid function tests

transcobalamin II, abnormal

transcobalamin II, hereditary absence of

transglutaminase antibodies

treatment of neurologic disorder

vascular endothelial growth factor

vasculitides

vasculopathy

vegetarianism

Venereal Disease Research Laboratory test

venous thrombosis, non-cerebral

vertigo

vibratory sensation, abnormal

violent behavior

visual evoked response

vitamin supplementation

vitamin therapy

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Wernicke's encephalopathy

word-finding difficulty

workup

writing

Showing articles 750 to 800 of 1264 << Previous Next >>

Cerebral Artery Aneurysms in Children Infected with Human Immunodeficiency Virus
J Pediatr 121:927-930, Husson,R.N.,et al, 1992

Wernicke's Encephalopathy and Central Pontine Myelinolysis Associated with Hyperemesis Gravidarum
BMJ 305:517-518, Bergin,P.S.&Harvey,P., 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Neurologic Syndrome in 25 Workers from an Aluminim Smelting Plant
Arch Int Med 152:1443-1448, White,D.M.,et al, 1992

Gastrointestinal Dysfunction in Parkinson's Disease:Frequency and Pathophysiology
Neurol 42:726-732, Edwards,L.L.,et al, 1992

Long-Term Outcome of Neonatal Meningitis
Am J Dis Child 146:567-571, Franco,S.M.,et al, 1992

Postneonatal Vitamin B6-Dependent Epilepsy
Pediatr 90:221-223, Coker,S.B., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
Pediatrics 89:768-770, Labrune,P.H.,et al, 1992

Factors Impairing Daytime Performance in Patients with Sleep Apnea/Hypopnea Syndrome
Arch Int Med 152:538-541, Cheshire,K.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Cognitive and Motor Development in Infants at Risk for Human Immunodeficiency Virus
Am J Dis Child 146:218-222, Aylward,E.H.,et al, 1992

Encephalitis in Cat Scratch Disease with Persistent Dementia
JNNP 55:133-135, Revol,A.,et al, 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Cognitive Functioning in Cancer Patients:Effect of Previous Treatment
Neurol 42:434-436, Meyers,C.A.&Abbruzzese,J.L., 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Is Aluminium a Dementing Ion?
Editorial, Lancet 339:713-7141992., , 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Cognitive Development of Yu-Cheng ('Oil Disease') Children Prenatally Exposed to Heat-Degraded PCBs
JAMA 268:3213-3218, Chen,Y.J.,et al, 1992

Chemotherapy for Acute Lymphocytic Leukemia:Cognitive and Academic Sequelae
J Pediatr 121:885-889, Brown,R.T.,et al, 1992

Central Nervous System Involvement in the Eosinophilia-Myalagia Syndrome
Arch Neurol 49:1082-1085, Lynn,J.,et al, 1992

Chronic Encephalitis (Rasmussen's Syndrome) and Ipsilateral Uveitis
Ann Neurol 32:826-829, Harvey,A.S.,et al, 1992

Prevention of First Occur of Neural-Tube Defects by Periconceptional Vitamin Suppl
NEJM 327:1832-1835, 18751992., Czeizel,A.E.&Dudas,I., 1992

Intellectual Development at Age 12 Years of Children with Congen Hypothyroidism Diag by Neonatal Scr
J Pediatr 121:581-584, Glorieux,J.,et al, 1992

Low-Level Lead Exposure, Intelligence and Academic Achievement:A Long-Term Follow-Up Study
Pediatrics 90:855-861, Bellinger,D.C.,et al, 1992

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Clinical Outcome in Aggressively Treated Meningeal Gliomatosis
Neurol 42:252-254, Grant,R.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Cerebral Infarction Associated with Protein C Deficiency
Stroke 23:108-111, Matsushita,K.,et al, 1992

Hypoglycemia Presenting as Basilar Artery Thrombosis
Stroke 23:112-113, Rother,J.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Pre-and Postcontrast MR Studies in Tuberous Sclerosis, Wippold
J Comput Assist Tomogr 16:69-72, II,F.J.,et al, 1992

Multiple Sclerosis Dementia
Neurol 42:696, Mendez,M.D.&Frey,W.F., 1992

Event-Related Potential P300 in MS, Relation to Magnetic Resonance Imaging and Cognitive Impairment
Arch Neurol 49:44-50, Honig,L.S.,et al, 1992

Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
J Pediatr 120:740-746, Autti-Ramo,I.,et al, 1992

Cognitive Abilities & School Performance of Extremely Low Birth Weight Children & Matched TermControls at Age 8
J Pediatr 118:751-760, Saigal,S.,et al, 1991

Effect of Very Low Brith Weight and Subnormal Head Size on Cognitive Abilities at School Age
NEJM 325:231-237, Hack,M.,et al, 1991

Prevention of Neural Tube Defects:Results of the Medical Research Council Vitamin Study
Lancet 338:131-137, 153-1541991., , 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease
J Pediatr 119:42-45, Riviello,J.J.,et al, 1991

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Showing articles 750 to 800 of 1264 << Previous Next >>