Neudle.com: "familial brain tumor"

Differential
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abducens nerve paralysis

abscess, intracerebral

abulia

acid maltase deficiency

acoustic nerve

acoustic nerve, vestibular division of

acoustic neurinoma

acoustic neurinoma, bilateral

acute disseminated encephalomyelitis

advances in neurology

aggression

akinetic mute

alcohol intolerance

alcohol, neurologic complications with

algorithm

alkylating agents

altered states of consciousness

alternating rapid movement, impaired

alternative medicine

Alzheimer's disease

Alzheimer's disease, familial

aneurysm, intracranial

aneurysm, intracranial, familial

Angelman syndrome

angiofibroma, facial

angiomyolipomas

antibiotic prophylaxis

antimetabolite

anxiety

aphasia

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

ataxia telangiectasia

auditory evoked brainstem potentials

autism

autism, screening for

autonomic dysfunction

basal ganglia, lesion, bilateral

behavior

behavior, combative

behavioral disorder

benign essential tremor

biologic markers

blood dyscrasias, neurologic findings with

brachycephaly

brain scan, abnormal

brainstem, dysfunction

brainstem, neoplasms of

cafe au lait spots

calcarine artery

calcification, intracranial

carcinoma of pancreas

CAT scan, contrast enhanced

cataracts

caudate nucleus, atrophy

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar lesion

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral embolism

cerebral infarction, subcortical

cerebral palsy

cerebral venous infarction

cerebral venous thrombosis

cerebroretinal vasculopathy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, neonatal

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

chest x-ray, abnormal

children

chorea

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

congenital myopathy

constipation

contraindications

conus medullaris, lesion of

corpus callosum, lesion of

cough

Cowden syndrome

cranial nerve tumor

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

Creutzfeldt-Jakob disease, genetic

crossed adductor reflex

cyanosis

cyst

cyst, peritumoral

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cytomegalovirus infection

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, familial

dementia, rapidly progressive

dementia, thalamic

dentate nuclei

dentate nuclei, lesion of

developmental disability

developmental evaluation

developmental retardation

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

dilantin

diplopia

disability rating scale, neurological

dizziness

drooling

dropped head syndrome

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electromyogram

ELISA

embolism, paradoxical

encephalitis

encephalitis, viral

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

endocarditis, prophylaxis

endolymphatic sac tumors

ependymoma

epidemiology of neurology

epidermoid

epileptic encephalopathy

epistaxis

epistaxis, recurrent

everolimus

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

fibrinolytic agents, contraindications

fibroma, ungual

fibromuscular dysplasia

finger nose finger test

fish

floppy infant

fluorescene in situ hybridization

Friedreich's ataxia, late onset

frontal balding

fundus, abnormality of

genetic neurologic disorders

genetic screening

genetic testing

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

globus pallidus, lesion of, bilateral

glutaric acidemia

granulomatosis with polyangiitis

granulomatous disease

Hallervorden Spatz disease

hearing loss, sudden, unilateral

hematopoietic tissue, extramedullary

hematuria, gross

hemianopia

hemianopia, homonymous

hemiparesis

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hepatic failure

hepatitis

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

hiccoughs

high arched palate

homocystinuria

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, communicating

hypopigmentation of skin

hypotonia

hypotonia, infants

hypoxia

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

imbalance

immunodeficiency

impotence

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

intellectual deterioration

intracerebral hemorrhage

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intraventricular hemorrhage

iris, abnormal

iron, brain

isoniazid

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw pain

karyotyping

Korsakoff's psychosis

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukopenia

level of consciousness, decreased

Lhermitte-Duclos disease

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

macrocephaly

macrognathia

magnetic susceptibility

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

maple syrup urine disease

medulla oblongata, neoplasm of

medulloblastoma

memory, impairment of

meningitis, carcinomatous

meningoencephalopathy

mental retardation

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

methotrexate

methylhydrazine derivatives

metronidazole

microcephaly

microhemorrhage, intracerebral

mitral valve prolapse

molecular genetics

mongolism

monoamine oxidase inhibitors

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, fetal

MRI, functional

MRI, gradient-echo

MRI, incidental finding

MRI, negative

MRI, paramagnetic effect

MRI, punctate pattern

MRI, ring sign

MRI, spinal cord

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

myelinolysis, extrapontine

myotonia dystrophica, classification

nausea and vomiting

neck weakness

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, intracranial

neoplasm, intracranial, multiple

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracerebral, reoperation

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS assoc.with primary malig.other sites

neoplasm, primary of CNS-aged

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-multiple

neoplasm, primary of CNS-recurrent

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve growth factor

neurocutaneous disease

neurodegeneration with brain iron accumulation

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neuronal migration disorder

neuropathology

neuropathy

neuropathy, peripheral

neurotoxin

nevoid basal cell carcinoma syndrome

nevus

newborn, evaluation of

next-generation sequencing

nitrogen mustard

Notch3 gene

nystagmus

nystagmus, dissociated

optic neuritis, bilateral

orthostatic hypotension

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paraplegia

paresthesias

Parkinson disease

Parkinson disease, surgical treatment of

Parkinsonism syndrome

patient information and support

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

polycystic kidneys

polycythemia, primary

polymerase chain reaction

polyps, gastrointestinal tract

pregnancy, neurologic complications in

premature infant

prevention of neurologic disorders

procarbazine

prognathism

prognosis

progressive neurologic disorder

proprioception, abnormal

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosocial aspects

ptosis

ptosis, bilateral

pulmonary infiltrates

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rash

real-time quaking-induced conversion

recombinant DNA

remote effect of cancer on the nervous system

renal cell carcinoma

renal cyst

renal failure

reticulum cell sarcoma

rhabdomyosarcoma of heart

rigidity

risk factors

root lesion, nerve

saccadic eye movements, abnormal

seizure, complications following

seizure, diagnosis of

seizure, etiology of

seizure, familial

seizure, neonatal

seizure, treatment of

skin, lesions in neurologic disorders

skull x-ray, abnormal

speech disorder, childhood

speech, delayed development of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, meningioma

spinal cord, neoplasm, neurofibroma

spinal muscular atrophy

spine, metastasis to

spinocerebellar degeneration

stem cell transplantation

stereotaxic surgery

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stimulation, deep brain

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subependymal nodules

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, protrusion of

top of the basilar syndrome

transient ischemic attack

transposition of the great vessels

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

trinucleotide repeats

tuber, cortical

tuberin

tuberous sclerosis

tuberous sclerosis, screening for

tumor suppressor gene

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking frame

walking, difficulty with

weakness

web sites

weight loss

Wernicke's encephalopathy

wheelchair

white freckles

white matter disease

white matter disease, subcortical

X-linked bulbospinal neuronopathy

Showing articles 0 to 50 of 17091 Next >>

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
Adams & Victors Principles of Neurology, Chp 31, pg 656, Ropper, A.H.,et al, 2014

Tremor
JAMA 311:948-954, Elias, W.J. & Shah, B.B., 2014

Efficacy and Safety of Everolimus for Subependymal Giant Cell Astrocytomas Associated with Tuberous Sclerosis Complex (EXIST-1): A Multicenter, Randomized, Placebo-Controlled Phase 3 Trial
Lancet 381:125-132, Franz, D.,et al, 2013

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Familiality in Brain Tumors
Neurol 71:1015-1020, Blumenthal,D.T.&Cannon-Albright,L.A., 2008

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Primary Brain Tumours in Adults
Lancet 361:323-331, Behin,A.,et al, 2003

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999

Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
neurol 44:1083-1086, Lasser,D.M.,et al, 1994

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992

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

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
Neurol 41:1923-1927, Pulst,S.M.,et al, 1991

Brain Tumors
NEJM 324:1471-1476, 1555-15641991., Black,P.McL., 1991

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Clinicopath Conf
Pheochromocytoma of Adrenal Gland, Von Hippel-Lindau Disease, Case 16-1991, NEJM 324:1119-112791., , 1991

Familial Meningioma
Neurol 40:312-314, McDowell,J.R., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Occurrence of Both Neurofibromatosis 1 and 2 in the Same Individual with a Rapidly Progressive Course
Neurol 39:282-283, Sadeh,M.,et al, 1989

Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
Neurol 39:487-492, Baptiste,M.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Showing articles 0 to 50 of 17091 Next >>