Neudle.com: "x-linked intellectual deficit"

Differential
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abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

Addison's disease

adducted thumb

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

affect, inappropriate

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anemia

antibiotics

antithyroid antibodies

attention deficit disorder with hyperactivity

autism

autoantibodies

autonomic dysfunction

Babinski sign

bacterial infection

Balint's syndrome

basal ganglia, calcification of

basilar impression

Bassen-Kornzweig syndrome

behavioral disorder

bilateral periventricular nodular heterotopia

bone density, increased

bone marrow transplantation

calcification, intracranial

carcinoma

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

CAT scan, brain scan compared to

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, false negative

CAT scan, hare's ears sign on

cataracts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebral cortical atrophy

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, pressure increased

cerebrovascular accident

Chamberlane's line

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

children

chromosomal abnormality

chromosome 28

Clinical Pathologic Conference(C.P.C.)

color vision, impaired

confusion

congenital malformation

controversies in neurology

cornea, abnormal

cornea, opacity of

corpus callosum, hypoplastic

cortical blindness

cost effectiveness

counselling

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

cyst, arachnoid, infant

cyst, benign intracranial

degenerative diseases of CNS

dementia

dementia, childhood

dementia, presenile

dementia, rapidly progressive

demyelinating disease

depression

developmental evaluation

developmental milestones, loss of

developmental retardation

diabetes insipidus

diarrhea

differential diagnosis

digits, abnormal

diplopia

disability, neurological

disorientation

dizziness

DNA probes

drug induced neurologic disorders

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalitis

encephalitis, autoimmune

encephalopathy

evoked potentials

exome sequencing

eye movement, disorders of

face, elongated

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal lobe, pathologic signs of

fundus, abnormality of

gait disorder

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

granulomatous disease

grasp reflex

growth retardation

Guillain Barre syndrome

gum disease

Hallervorden Spatz disease

Hand-Schuller-Christian disease

head circumference

head injury

head injury, prognosis in

headache

hearing loss

hearing problems in children

hemiatrophy

hemiparesis

hemoglobin abnormality, neurologic complications of

hepatomegaly

hepatosplenomegaly

heralding manifestation

heterotopia

hirsutism

hoarseness

Hodgkin's disease, neurologic involvement with

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, normal pressure

hyperactivity

hyperostosis

hyperostosis corticalis generalisata familiaris

hyperpigmentation of skin

hypocalcemia

hypoglycorrhachia

hypoparathyroidism, idiopathic

hypotonia

imbalance

immunohistochemistry

immunosuppressive agents

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

infantile spasm

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal biopsy

intracranial hemorrhage

intracranial pressure, increased

intrathecal chemotherapy

irritability

joint hypermobility

karyotyping

Kearns-Sayre syndrome

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

lymphadenopathy, hilar

lymphocyte fingerprint profiles

lymphoma

lymphoma involving CNS

macrocephaly

macular degeneration

malformation, CNS, congenital

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, granulomatous

meningitis, lymphomatous

meningitis, rheumatoid

meningoencephalitis

mental retardation

mental retardation, etiology of

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

microcephaly

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, spinal cord

mucopolysaccharidoses

multinucleated giant cell

multiple system atrophy

muscle biopsy

muscle pain

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

myopathy, mitochondrial

myopia

nausea and vomiting

neck pain

necrotizing granuloma

neonatal screening, genetic neurologic disorders

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

neuroendocrinology

neurofibromatosis 1

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, peripheral

old age, neurology of

oligophrenin 1

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic atrophy, infants

optic foramina

optic foramina, abnormal

optic nerve

optic neuropathy

osteolytic lesion, causes of

paraparesis, familial spastic

paraparesis, spastic

Parkinsonism syndrome

paroxysmal nonkinesigenic dyskinesia

photosensitivity, skin

pigmentary retinopathy

pineal, shifted

pituitary stalk

pituitary stalk, lesion of

pituitary, enlargement

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

pneumothorax

polymerase chain reaction

port wine nevus

posterior fossa, mass of

practice guidelines

precocious puberty

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

pseudarthrosis

pseudobulbar palsy

psychiatric disorder

psychological testing

psychomotor retardation

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

remote effect of cancer on the nervous system

respirations in CNS disease

reticulum cell sarcoma

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

sensorineural hearing loss

serologic testing

short stature

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

skin, lesions in neurologic disorders

skull fracture

skull x-ray

skull x-ray, abnormal

skull x-ray, bony defect on

somatosensory evoked potentials

Southern immunoblot test

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar degeneration

splenomegaly

steroid therapy, CNS treatment and complications with

stimulant drugs

Sturge-Weber syndrome

subdural hematoma

subdural hematoma, bilateral

symmetric brain lesions

syndactyly

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

testicular enlargement

thalassemia

thalassemia/mental retardation syndrome

thrombocytopenia

tinnitus

toxins, nervous system

toxoplasmosis, CNS

transilumination of skull

treatment of neurologic disorder

trinucleotide repeats

very long chain fatty acids

Virchow-Robin spaces, dilated

visual acuity, decreased

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked intellectual deficit

X-linked lissencephaly

x-linked mental retardation

Showing articles 0 to 50 of 5853 Next >>

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Sarcoidosis Limbic Encephalitis
Iran J Neurol 16:156-158, Toudou-Daouda, M.,et al, 2017

MRI in X-Linked Adrenoleukodystrophy
Neurol 84:211, Siddiqui, S.,et al, 2015

Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Newborn Screening for Fragile X Syndrome
JAMA Neurol 71:355-359, Tassone, F., 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Granulomatous Meningitis due to Rheumatoid Arthritis
Acta Neurol Belg 112:193-197, Duray, M.C.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Oligophrenin 1 Mutations Frequently Cause X-Linked Mental Retardation with Cerebellar Hypoplasia
Neurol 65:1364-1369,1346, Zanni,G.,et al, 2005

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Mental Retardation
Neurol 61:156-157, Patterson,M.C. &Zoghbi,H.Y., 2003

Practice Parameter: Evaluation of the Child with Global Developmental Delay
Neurol 60:367-380, Shevell,M.,et al, 2003

New Strategy for Prenatal Diagnosis of X-Linked Disorders
NEJM 346:1502, Costa,J.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
Ann Neurol 42:360-364, Claes,S.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Intelligence and the X Chromosome
Lancet 347:1814-1815, Turner,G., 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
J Pediatr 127:193-199, Majnemer,A.&Shevell,M.I., 1995

Rapid Antibody Test for Fragile X Syndrome
Lancet 345:1147-1148, Willemsen,R.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Do Young Boys with Fragile X Syndrome have Macroorchidism
Pediatrics 93:992-995, Lachiewicz,A.M.&Dawson,D.V., 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Presenile-Onset Cerebral Adrenoleukodystrophy Presenting as Balint's Syndrome and Dementia
Neurol 43:1249-1251, Uyama,E.,et al, 1993

X-Linked Adrenoleukodystrophy:Adult Cerebral Variant
Neurol 43:1518-1522, Farrell,D.F.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

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

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

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

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
NEJM 325:1720-1738, Sutherland,G.R.,et al, 1991

More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation
Lancet 338:1562-1563, , 1991

Mental Retardation in Turner Syndrome
J Pediatr 118:415-417, VanDyke,D.L.,et al, 1991

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Encephalotrigeminal Angiomatosis
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 582, Gold,A.P., 1989

Short-Term Outcomes of Skull Fracture:A Population-Based Study of Survival and Neurologic Complications
Neurol 39:96-102, Wiederholt,W.C.,et al, 1989

Showing articles 0 to 50 of 5853 Next >>