About: Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study

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scientific article published on 01 October 1983

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1983 (uk) im Oktober 1983 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 October 1983 (en) artículu científicu espublizáu n'ochobre de 1983 (ast)
publication date	wds:Q70180906-C75DFED5-3E66-4285-8BD0-C0104D42C84A
publication date	1983-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q70180906-166BB9AB-2B10-49F5-8EE9-10A6AC205334 wds:Q70180906-60BBDF8C-1338-40B9-8BC3-8313CFEFEC45 wds:Q70180906-B01111A0-5E5A-4AAF-A5DD-0049D07E5152 wds:Q70180906-CE4E4282-147B-4D5F-BF47-F9583392A7D9 wds:Q70180906-DB7DC65A-5421-46D6-A98C-5DE398B785CF
author name string	R Gherardi F Lhermitte P Castaigne H P Cathala P Bouché
rdfs:label	Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (en) Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (nl)
skos:prefLabel	Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (en) Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (nl)
name	Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (en) Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (nl)
title	wds:Q70180906-0108A021-B2B0-4D30-8FE9-89CA6ECE80B9
title	Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study (en)
page(s)	wds:Q70180906-40C5F847-0785-4367-914A-294039B1AA79
page(s)	389-399
instance of	wds:Q70180906-93F51C3A-EF8F-4677-AE98-DE453E3366E5
instance of	scholarly article
PubMed ID	wds:Q70180906-F89618A3-C3BF-4370-B834-704FC73CA818
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6317809
PubMed ID	6317809
published in	wds:Q70180906-187D0526-F8E8-4237-A02D-788B74CED310
published in	Journal of the Neurological Sciences
issue	wds:Q70180906-A53CB764-DCC2-40CC-8CA9-B4236BF5F2FE
volume	wds:Q70180906-0933AFA3-F0A1-433C-A25C-96813183E3F3
issue	3
volume	61
DOI	wds:Q70180906-27B2B8DB-23F5-44CA-936C-863F08AD150E
DOI	http://dx.doi.org/10.1016/0022-510X(83)90172-7
DOI	10.1016/0022-510X(83)90172-7
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70180906
is cites work of	Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis. The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and management Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma Somatosensory evoked potentials, sensory nerve potentials and sensory nerve conduction in hereditary motor and sensory neuropathy type I. Estimation of the inbreeding coefficient through use of genomic data Intermediate forms of Charcot-Marie-Tooth neuropathy: a review NEFL N98S mutation: another cause of dominant intermediate Charcot-Marie-Tooth disease with heterogeneous early-onset phenotype NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype. A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplication An essential role of MAG in mediating axon-myelin attachment in Charcot-Marie-Tooth 1A disease Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity Genetic linkage studies in hereditary motor and sensory neuropathies Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease Comparison of CMT1A and CMT2: similarities and differences Molecular genetics of charcot-marie-tooth disease: from genes to genomes New insights into the pathophysiology of pes cavus in Charcot-Marie-Tooth disease type 1A duplication The leakage of serum proteins across the blood-nerve barrier in hereditary and inflammatory neuropathies. An immunohistochemical and morphometric study Hereditary motor and sensory neuropathy type I and type II. A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review [Electrophysiological study of a family of subjects presenting primary hypertrophic neuritis] [Electrophysiological studies in the assessment of polyneuropathies] Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases
is cites work of	wds:Q31030793-407BFC6D-C68F-4CF1-BD38-FAE7A3ECCEFC wds:Q33845744-9C19E9AC-474A-43A2-8C8C-014E59850165 wds:Q36507157-10C1F1F1-29E7-42F9-AEB6-450B9C04F247 wds:Q79139583-CE532C60-41A3-4FE2-9388-2F4C2587E959 wds:Q29029240-E913AB89-8C2F-4179-9FFA-9279630A6E64 wds:Q34400945-40D6248F-BEB9-4F84-86A8-3E3E73BA7267 wds:Q36081783-0B9F02B3-37F1-413F-9385-4452A7875887 wds:Q36493294-A679E691-BA37-42A5-8B0C-400F3EAE2170 wds:Q37876789-BFB873EB-28CD-4724-B743-13B3384F6ACB wds:Q50448017-F79834C6-89A2-4AF0-9E69-19C5EE4992E5 wds:Q26777319-D60BFE70-DD99-4F10-82EC-8F8E607FDC0A wds:Q67922224-3A634C8C-EBA5-44DB-8EAF-11CEEFF5F77C wds:Q93955870-6B2F4369-3313-4785-AE62-908F91C25F9D wds:Q38917040-96FF0624-BA1D-481B-BCD4-5127243F2CAE wds:Q43857957-4AFC4DCE-796B-47E8-A1C8-F9A665C3C8A2 wds:Q24532011-8012BFA8-195A-4804-9A25-92D49F7D30A7 wds:Q41217658-2B192A69-5EE1-4BBC-BF03-1D8D06D606E5 wds:Q37697478-E9219E16-6FF9-4F2F-9A3A-C6F21F732734 wds:Q69102329-622576C6-D977-4C6A-B621-DD23549564AE wds:Q68146350-9CC334F1-9390-4A80-97DC-2EB143CECA2B wds:Q68782641-15F58FD7-93A8-4906-AA53-5A39FFE84D14 wds:Q34044153-2A0FB55B-1B49-4C28-BA48-908CC07A4187 wds:Q39212369-7C70A79C-D6B1-44F2-B3EE-D8DC2F194381 wds:Q58183378-3EC52464-05DC-419D-9CAE-24DCA9AC971E wds:Q70151555-EB112132-A6BC-4FFB-B037-236B40856BF4 wds:Q30816457-E0439B03-7779-4C6A-9D49-4F1C88A72DFF

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