Neudle.com: "angiokeratoma corpis diffusum"

Differential
(Click to cross reference)

abdominal cramps

acral sensory symptoms

agalsidase alfa

algorithm

alpha galactosidase A deficiency

aneurysm, intracranial

aneurysm, intracranial, familial

angina pectoris

angiography, cerebral

angiography, posterior fossa

angiokeratoma

anhidrosis

aortic arch ulcerated plaques

autonomic dysfunction

basal ganglia, calcification of

basilar artery occlusion

brainstem, infarction of

burning feet

burning feet, differential diagnosis of

burning hands

burning paresthesia

calcification, intracranial

cancer, cerebrovascular accident complicating patients with

central nervous system, infection of

central pontine myelinolysis

cerebellar infarction

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral embolism

cerebral infarction, subcortical

cerebral ischemia

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, etiology

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, without occluded vessel

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

children

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

coagulopathy

cognition

congestive heart failure

cornea, abnormal

cornea, opacity of

corneal dystrophy

corpus callosum, lesion of

dementia, rapidly progressive

diarrhea

differential diagnosis

diplopia

dysarthria

echocardiogram

ectatic basilar artery

edema, pedal

efficacy

Ehlers-Danlos syndrome

electron microscopy

embolic stroke of unknown source

fibromuscular dysplasia

genetic neurologic disorders

genetic screening

genetic testing

glioma

globus pallidus, lesion of, bilateral

hand pain

headache

headache, thunderclap

hearing loss

heat intolerance

hemianopia, homonymous

hemiparesis

hemoglobin abnormality, neurologic complications of

hemorrhoids

hepatolenticular degeneration(Wilson's disease)

hereditary hemorrhagic telangiectasia(HHT)

homocystinuria

hydronephrosis

hypercoagulable state

hypertension

hypohidrosis

inborn errors of metabolism

intellectual deficit

intracerebral hemorrhage

intracerebral hemorrhage, young adult

Jakob-Creutzfeldt disease

lacunar infarction

Leigh's disease

leukocyte enzyme abnormality

leukodystrophy

lipid storage disorder of CNS

lymphadenopathy

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

marihuana

memory, impairment of

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

microhemorrhage, intracerebral

migraine

migraine, hemiplegic

mitral valve prolapse

MRI, diffusion weighted

MRI, gradient-echo

MRI, high signal foci on

MRI, T1 weighted high signal foci

multiple sclerosis, differential diagnosis of

muscular dystrophy, Duchenne

myocardial infarction

neoplasm, primary of CNS

nerve conduction studies

neurocutaneous disease

neurofibromatosis 1

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuropathic pain scale

neuropathology

neuropathy

neuropathy, painful

neuropathy, peripheral, treatment

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neurosis

next-generation sequencing

nystagmus

osmotic demyelination syndrome

pain

pain, head

pain, neuropathic

Parkinsonism syndrome

patent foramen ovale

polycythemia, primary

pons, lesion of

precipitating factors

prenatal diagnosis by amniocentesis

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

respiratory tract infection

sensorineural hearing loss

sick sinus syndrome

sickle cell disease

skin, biopsy

skin, lesions in neurologic disorders

slit lamp examination

small vessel disease

small vessel disease, cerebral

splenomegaly

subarachnoid hemorrhage

sweating, abnormality of

symmetric brain lesions

systemic illness

Tay-Sachs disease

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tinnitus

treatment of neurologic disorder

vertebral-basilar insufficiency

vertigo

vertigo, episodic

visual loss

visual loss, transient

Von Hippel Lindau

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

workup

Showing articles 0 to 28 of 28

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

Redefining the Pulvinar Sign in Fabry Disease
AJNR 38:2264-2269, Cocozza, S.,et al, 2017

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Embolic Strokes of Unknown Source and Cryptogenic Stroke: Implications in Clinical Practice
Front Neurol 7:1-16, Nouh, A.,et al, 2016

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Inherited Metabolic Diseases of the Nervous System, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data
Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Enzyme Replacement Therapy Improves Function of C-, Adelta-, and Abeta- Nerve Fibers in Fabry Neuropathy
Neurol 62:1066-1072, Hilz,M.J.,et al, 2004

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

T1 Hyperintensity in the Pulvinar: Key Imaging Feature for Diagnosis of Fabry Disease
AJNR 24:916-921, Takanashi,J.,et al, 2003

Increased Signal Intensity in the Pulvinar on T1-Weighted Images: A Pathognomonic MR Imaging Sign of Fabry Disease
AJNR 24:1096-1101, Moore,D.F.,et al, 2003

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Enzyme Replacement Therapy in Fabry Disease
JAMA 285:2743-2749, Schiffmann,R.,et al, 2001

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Nervous System Involvement in Fabry's Disease:Clinicopath & Biochemical Correlation
Ann Neurol 23:505-509, Kaye,E.M.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

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

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57
1974., , 1974

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

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

Showing articles 0 to 28 of 28