Neudle.com: B 12 deficiency

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Differential
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abdominal distention

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

Addison's disease

adverse drug reaction

affective disorders

alcoholic polyneuropathy

aminoacidopathies

amyloid angiopathy, cerebral

anemia, hemolytic

anemia, iron deficiency

anemia, megaloblastic

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anticonvulsants, untoward effects of

antiendomysial antibodies

arterial dissection, precipitating events

ascending paralysis

ataxia, cerebellar

ataxia, sensory

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

B 12 deficiency, infants

B 12 metabolism, defective

B12 binding protein, abnormal

bacterial infection

basal ganglia, lesion of

Behcet's syndrome

blood dyscrasias, neurologic findings with

burning feet, differential diagnosis of

burning paresthesia

carbon monoxide poisoning

carcinoma of pancreas

carotid artery disease

carotid artery stenosis

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 injury

cervical spondylosis

chemotherapy, CNS treatment and complications with

chorea, causes of

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

collagen vascular disease

concentration, impaired

congestive heart failure

controversies in neurology

copper deficiency

corpus callosum

corpus callosum, lesion of

cortical blindness

C-reactive protein, elevated

Cushing's syndrome

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

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

differential diagnosis

dilantin, toxicity

disability, neurological

dissociated sensory loss

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dystonia, focal

electrical sensation

electroencephalogram

electrophoretic pattern, serum

emotional lability

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy, Hashimoto's

epidemiology of neurology

evidence-based research

evoked potentials

failure to thrive

fine motor function, impaired

folic acid deficiency

F-wave response

gastrectomy, neurologic complications following

gastric partitioning

gastric surgery

gastrointestinal disease, neurologic complications

genetic neurologic disorders

genetic testing

girdle sensation

gliadin antibodies

gliomatosis cerebri

glucose level, serum

glucose tolerance test, abnormal

gluten sensitivity

gluten-free diet

hallucination, auditory

helicobacter pylori

hemorrhagic diathesis

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

hip flexor weakness

histamine-2 receptor blockers

homocysteine, serum

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

hyperadrenalism

hyperbilirubinemia

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hypertensive encephalopathy

hyperthyroidism

hypoparathyroidism

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hypotonia, infants

iatrogenic neurologic disorders

incontinence, fecal

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

inverted V sign

iron, serum, low

laboratory values, normal

lactic dehydrogenase(LDH)

leg weakness, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lhermitte's sign

limbic encephalitis

liver function enzymes

long bone lesion

lymphoma involving CNS

lymphoma, primary of CNS

malabsorption syndrome

memory, defect of recent

memory, impairment of

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

methylmalonic acid, serum

methylmalonic acidemia

midbrain, lesion of

Mini Mental Status Examination

mitochondrial disease

monoclonal gammopathy

movement disorder

movement disorder, extrapyramidal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

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, tract-specific

myelopathy, vacuolar

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neural tube defect

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuropathy, diabetic

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

newborn, evaluation of

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

old age, neurology of

optic neuritis, etiology of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, nutritional

orthostatic hypotension

pain, abdominal

pain, neuropathic

paraparesis, spastic

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

personality change

phenothiazine, dyskinesia associated with

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

plasma R binder deficiency

polyradiculoneuropathy

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

posterior tibial nerve

posterior tibial nerve compression

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

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

psychosis, acute

psychosis, cause of

psychotic behavior

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

radiation therapy, CNS treatment and complications with

regional enteritis

remote effect of cancer on the nervous system

retinal hemorrhages

reversible neurologic disorder

sarcoidosis, CNS

sclerosis, bone

scotoma, central

sensory loss, cutaneous

sensory loss, glove-stocking

sickle cell disease

skin, darkening of

skin, discoloration

skin, lesions in neurologic disorders

somatosensory evoked potentials

speech, pressured

spinal cord, cervical

spinal cord, lesion of

substantia nigra

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tarsal tunnel syndrome

thiamine deficiency

thyroid function tests

tongue, swelling

transcobalamin II, abnormal

transcobalamin II, hereditary absence of

transglutaminase antibodies

treatment of neurologic disorder

tremor, orthostatic

ulcerative colitis

urinary incontinence

vascular endothelial growth factor

Venereal Disease Research Laboratory test

vibratory sensation, abnormal

visual evoked response

visual loss, slow

vitamin D deficiency

vitamin deficiency

vitamin supplementation

vitamin therapy

walking, difficulty with

weakness, generalized

weakness, progressive

Wernicke's encephalopathy

Whipple's disease

white matter disease

wide based gait

word-finding difficulty

Showing articles 1650 to 1700 of 1819 << Previous Next >>

Primary Intracranial Lymphoma of the Dura
Arch Neurol 37:528-529, Jazy,F.K.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Extramedullary Hematopoiesis & Spinal Cord Compression Complicating Polycythemia Rubra Vera
Ann Neurol 7:81-84, Rice,G.P.A.,et al, 1980

Clin. Path. Conference
Lymphoplasmacytic Intersitial Pneumonitis, Progressive Multifocal Leukoencephalopathy. Case Record 1, -10,NEJM 302:795,1980., 1980

Diagnosis of Cryptococcal Meningitis by Cytologic Methods:An Old Technique Revisited
Neurol 30:102-105, Bernard,P.G.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Cerebral Infarcts with Arterial Occlusion in Neonates
Ann Neurol 6:495-502, Barmada,M.A.,et al, 1979

Deficiency of Arylsulfatase B in 2 Brothers Aged 40 & 38 Years (Maroteaux-Lamy Syndrome, Type B)
Ann Neurol 6:315-325, Pilz,H.,et al, 1979

Iatrogenic Night Blindness & Keratoconjunctival Xerosis
NEJM 301:943-944, Partamian,L.G.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

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

Periodic Lateralized Epileptiform Discharges in Infants & Children
Ann Neurol 6:47-50, PeBenito,R.,et al, 1979

Bilateral Rhinocerebral Phycomycosis
Ann Neurol 6:131-133, Kasper,L.H.,et al, 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Progressive Myelopathy Due to Extramedullary Hematopoiesis:Case Report & Review of the Literature
Ann Neurol 5:485-489, Stahl,S.M.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Fetal Alcohol Syndrome & Related CNS Problems
Neurol 29:1429-1430, Wisniewski,K.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

A Comparison of Amphotericin B Alone & Comb. With Flucytosine in the Treatment of Cryptoccal Meningitis
NEJM 301:126, Bennett,J.E.,et al, 1979

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Status Epilepticus in Pregnancy:Effect of Phenytoin Malabsorption on Seizure Control
Neurol 28:85, Ramsay,R.E.,et al, 1978

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

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Hyperphenylalaninemia Due To A Deficiency of Biopterin
NEJM 299:673-679, Stanley,S.K.,et al, 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Polyneuropathy & Folate Deficiency
Arch Neurol 35:581-584, Botez,M.I.,et al, 1978

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

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

The Role of Judges in Life/Death Decision for the Neurologically Impaired
Ann Neurol 4:463-464, Beresford,H.R., 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Cryptococcal Meningitis
Arch Neurol 35:179, Roberts,N.J.,et al, 1978

The Spectrum of Primary Blastomycotic Meningitis:A Review of Central Nervous System Blastomycosis
Ann Neurol 3:26, Gonyea,E.F., 1978

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

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

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Role of Magnesium Depletion in Wernicke-Korsakoff Syndrome
NEJM 298:743, Flink,E.B., 1978

Prevention of the Wernicke-Korsakoff Syndrome
NEJM 299:285, Centerwall,B.S.,et al, 1978

Marchiafava-Bignami Disease
Neurol 28:290, Koeppen,A.H.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Showing articles 1650 to 1700 of 1819 << Previous Next >>