HMSN I: Early Diagnosis

The value of nerve conduction velocities in the detection of hereditary motor sensory neuropathy type I (HMSN I) in children at risk was determined in 36 children under 10 years of age at the University of Western Ontario, London, Ontario, Canada.

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 1992-11-01
Series:Pediatric Neurology Briefs
Subjects:
Online Access:https://www.pediatricneurologybriefs.com/articles/3112
id doaj-d328d0c290ce4e758c9849d0f2de77ec
record_format Article
spelling doaj-d328d0c290ce4e758c9849d0f2de77ec2020-11-25T03:37:13ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64821992-11-01611868710.15844/pedneurbriefs-6-11-103098HMSN I: Early DiagnosisJ Gordon Millichap0Northwestern University Feinberg School of MedicineThe value of nerve conduction velocities in the detection of hereditary motor sensory neuropathy type I (HMSN I) in children at risk was determined in 36 children under 10 years of age at the University of Western Ontario, London, Ontario, Canada.https://www.pediatricneurologybriefs.com/articles/3112hereditary motor sensory neuropathy type ipes planusmyelin glycoprotein
collection DOAJ
language English
format Article
sources DOAJ
author J Gordon Millichap
spellingShingle J Gordon Millichap
HMSN I: Early Diagnosis
Pediatric Neurology Briefs
hereditary motor sensory neuropathy type i
pes planus
myelin glycoprotein
author_facet J Gordon Millichap
author_sort J Gordon Millichap
title HMSN I: Early Diagnosis
title_short HMSN I: Early Diagnosis
title_full HMSN I: Early Diagnosis
title_fullStr HMSN I: Early Diagnosis
title_full_unstemmed HMSN I: Early Diagnosis
title_sort hmsn i: early diagnosis
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 1992-11-01
description The value of nerve conduction velocities in the detection of hereditary motor sensory neuropathy type I (HMSN I) in children at risk was determined in 36 children under 10 years of age at the University of Western Ontario, London, Ontario, Canada.
topic hereditary motor sensory neuropathy type i
pes planus
myelin glycoprotein
url https://www.pediatricneurologybriefs.com/articles/3112
work_keys_str_mv AT jgordonmillichap hmsniearlydiagnosis
_version_ 1724546492578922496