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 50 to 100 of 5853 << Previous Next >>

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Neurological Manifestations in Three German Children with AIDS
Neuropediatrics 18:99-106, Biggemann,B.,et al, 1987

Clinicopath Conf
Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986

Preventive Screening for the Fragile X Syndrome
NEJM 315:607-609, Turner,G.,et al, 1986

Preventive Screening for Fragile X Syndrome
Editorial, Lancet 2:1191-11921986., , 1986

Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985

Fragile X Syndrome:Associated Neurological Abnormalities & Developmental Disabilities
Ann Neurol 18:665-669, Wisniewski,K.E.,et al, 1985

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

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Prenatal Diagnosis of Fragile X Chromosome
Lancet 1:99-100, Shapiro,L.R.,et al, 1982

The Fragile X-Chromosome Mental Retardation & Large Testes
Arizona Med 37:764-766, Hecht,F.,et al, 1980

X-Linked Mental Retardation
Am J Med Genet 7:407-415, Turner,G.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Heterozygous Expression Of X-Linked Mental Retardation & X-chromosome Marker fra (X) (q27)
NEJM 303:662-664, Turner,G.,et al, 1980

Idiopathic Hypoparathyroidism Presenting as Dementia
Neurol 29:393-394, Slyter,H., 1979

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

The"Hypernormal"CT Scan in Dementia:Bilateral Isodence Subdural Hematomas
Neurol 29:1522-1524, Jacobson,P.L.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Neurological Complications of Infantile Osteopetrosis
Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Sarcoidosis of the Central Nervous System
JNNP 36:1024, Douglas,A.C.,et al, 1973

Benign Intracranial Cyst, In Neurosurgery of Infancy & Childhood
(Ed) , 1969, Charles C. Thomas p. 179., Matson,D.D., 1969

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Multiple "Rings" in the Brain
BMJ 383:e077299, Li,Y.et al, 2023

Mortality and Causes of Death in Children with Cerebral Palsy with Scoliosis Treated with and without Surgery
Neurol 101:e1787-e1792, Ahonen,M.,et al, 2023

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

A 22-Year-Old Man with Multifocal Brain and Osseous Lesions
Neurol 101:1025-1031, Reddy,S.,et al, 2023

Tuberous Sclerosis Complex:Clinical Features
www.UptoDate.com, Dec, Randle,S., et al, 2023

Clinical,Neuroimaging,and Genetic Markers in Cerebral Amyloid Angiopatny-Related Inflammation:A Systematic Review and Meta-Analusis
Stroke 54:178-188, Theodorou,A.,et al, 2023

Lecanemab in Early Alzheimers Disease
NEJM 388:9-21,80, van Dyck,A.H.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Endovascular vs Medical Management for Late Anterior Large Vessel Occlusion With Prestroke Disability
Neurol 100:e751-e763, Siegler, J.E., et al, 2023

Hearing Aids and Cochlear Implants in the Prevention of Cognitive Decline and Dementia-Breaking Through the Silence
JAMA Neurol 80:127-128, Denham,M.W.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

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

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Glucose Hypermetabolism in the Basal Ganglia
Neurol 101:90-91, Kim,Y.E.,et al, 2023

Neurologic Manifestations of Long COVID Differ Based on Acute COVID-19 Severity
Ann Neurol 94:146-159, Giraldo,G.S.P.,et al, 2023

Toward Gerineuropalliative Care for Patients with Dementia
NEJM 389:775-778, Harrison,K.L.,et al, 2023

Showing articles 50 to 100 of 5853 << Previous Next >>