Neudle.com: "hypomelinosis"

Differential
(Click to cross reference)

acrochordon

acromicria

ataxia telangiectasia

autoimmune cerebellar ataxia

CAT scan, emission, abnormal

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

children

chromosomal abnormality

chromosome 15

chromosome 16

chromosome 9

Clinical Pathologic Conference(C.P.C.)

congenital malformation

conversion reaction

cranial neuropathy, multiple

developmental retardation

electroencephalogram, abnormalities of

electromyogram

encephalitis, autoimmune

epidemiology of neurology

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

fine motor function, impaired

fish

fluorescene in situ hybridization

foot drop

fundus, abnormality of

F-wave response

gadolinium

gait disorder

gammaglobulin therapy, intravenous

gene

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glutamic acid decarboxylase, antibody

glycosuria

gray hair

growth hormone deficiency

hemihypertrophy, congenital

hyperpigmentation of skin

hypopigmentation of skin

inborn errors of metabolism

meningeal enhancement

monoclonal gammopathy

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

myeloma, osteosclerotic

myelopathy

neoplasm, primary of CNS

nerve biopsy

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuroophthalmology

neuropathology

neuropathy

neuropathy, asymmetric

neuropathy, chronic

neuropathy, painful

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

nystagmus

nystagmus, rotary

nystagmus, spontaneous

peroneal nerve, lesion of

phakomatoses

phenylketonuria

phenylketonuria, adult onset

plasmacytoma

pleocytosis of cerebrospinal fluid

POEMS syndrome

poliosis

polyneuropathy, chronic inflammatory demyelinating

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

prenatal diagnosis by amniocentesis

prognathism

progressive neurologic disorder

psychosis

pulmonary infiltrates

rapidly progressing neurologic illness

rhabdomyosarcoma of heart

scleroderma

scleroderma, neurologic involvement with

skin, lesions in neurologic disorders

slurred speech

smiling

speech disorder

speech disorder, childhood

speech, delayed development of

spina bifida

spinal cord, lesion of

tongue, protrusion of

treatment of neurologic disorder

tremulousness

tuberculosis

tuberculosis, miliary

tuberin

tuberous sclerosis

tuberous sclerosis, screening for

uveitis

valium

vascular endothelial growth factor

vertigo

vision, blurred

visual acuity, decreased

vitiligo

Vogt-Koyanagi-Harada syndrome

weakness, generalized

Showing articles 0 to 24 of 24

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

MR Imaging of Vogt-Koyanagi-Harada Syndrome with Leptomeningeal Enhancement
AJNR 32:E169-E171, Lohman, B.D.,et al, 2011

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

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

Clinicopath Conf., Leprosy
NEJM 350:166-176, Case 1-2004, 2004

Diffusion-Weighted Imaging of White Matter Abnormalities in Patients with Phenylketonuria
AJNR 22:1583-1586, Phillips,M.D.,et al, 2001

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

Ash-Leaf Spots in Tuberous Sclerosis
NEJM 338:1887, Kurlemann,G.&Schuierer,G., 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Chronic Inflammatory Demyelinating Polyneuropathy Associated with Malignant Melanoma
Neurol 46:822-824, Bird,S.J.,et al, 1996

Skin Lesions of the Spinal Axis and Spinal Dysraphism:Fifteen Cases & Review of the Literature
Arch Pediatr Adolesc Med 148:740-748, McAtee-Smith,J.,et al, 1994

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

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

Cranial MR Imaging in Hypomelanosis of Ito
J Comput Assist Tomogr 14:981-983, Williams III,D.W.&Elster,A.D., 1990

Hypomelanosis of Ito, Wood's Light & Magnetic Resonance Imaging as Diagnostic Measures
Arch Neurol 43:848-850, Ardinger,H.H.&Bell,W.E., 1986

Hypomelanosis of Ito:Association with a Chromosomal Abnormality
Neurol 35:607-610, Miller,C.A.,et al, 1985

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981

White Spots in Tuberous Sclerosis
J Pediatr 77:587, Hurwitz,S.,et al, 1970

White Leaf-Shaped Macules-Earliest Visible Sign of Tuberous Sclerosis
Arch Derm 98:1, Fitzpatrick,T.,et al, 1968

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Neurological Manifestations of Scleroderma
The Georgetown Medical Bulletin, 18:1101964., O'Doherty,D.S., 1964

Showing articles 0 to 24 of 24