J Julien
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Explore the profile of J Julien including associated specialties, affiliations and a list of published articles.
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Recent Articles
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Rajabally Y, Vital A, Ferrer X, Vital C, Julien J, Latour P, et al.
J Peripher Nerv Syst
. 2001 Jul;
5(3):158-62.
PMID: 11442172
It is well known that patients with Charcot-Marie-Tooth (CMT) disease are liable to present with episodes of cortisone-responsive demyelination, and a superimposed inflammatory component has been suggested. We report a...
13.
Julien J, Denier C, Ferrer X, Ducros A, Saintarailles J, Lagueny A, et al.
J Neurol
. 2001 May;
248(3):209-14.
PMID: 11355155
We describe a peculiar form of late onset paroxysmal cerebellar ataxia including clinical features similar to episodic ataxia type 2 (EA2) but unresponsive to acetazolamide. Four unrelated patients were clinically...
14.
Vital C, Vital A, Lagueny A, Ferrer X, Fontan D, Barat M, et al.
Ultrastruct Pathol
. 2001 Feb;
24(6):363-9.
PMID: 11206333
The authors recently reexamined the peripheral nerve biopsies from 42 patients with chronic inflammatory demyelinating polyneuropathy (CIDP). There were 27 males and 15 females, aged from 9 to 84 years,...
15.
Vital A, Fontan D, Julien J, Talon P, Heron B, Routon M, et al.
J Peripher Nerv Syst
. 2000 Aug;
3(2):125-32.
PMID: 10959246
Two unrelated female cases of congenital insensitivity to pain with anhydrosis are presented. The first case was born from consanguineous parents. In both cases, onset of manifestation was observed in...
16.
Vital A, Lagueny A, Julien J, Ferrer X, Barat M, Hermosilla E, et al.
Acta Neuropathol
. 2000 Jul;
100(1):63-8.
PMID: 10912921
The possible occurrence of chronic inflammatory demyelinating polyneuropathy (CIDP) in association with an identified dysglobulinemic status is recognized and a causal relationship between the two has been suggested. We had...
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Stieber A, Gonatas J, Collard J, Meier J, Julien J, Schweitzer P, et al.
J Neurol Sci
. 2000 Feb;
173(1):63-72.
PMID: 10675581
Fragmentation of the Golgi apparatus (GA) of motor neurons was first described in sporadic amyotrophic lateral sclerosis (ALS) and later confirmed in transgenic mice expressing the G93A mutation of the...
19.
Lagueny A, Latour P, Vital A, Rajabally Y, Le Masson G, Ferrer X, et al.
Neuromuscul Disord
. 1999 Nov;
9(6-7):361-7.
PMID: 10545037
Morphological modifications were investigated in the peripheral nerve of three unrelated patients with CMT1B. In two patients, molecular genetic analysis showed an Arg98His mutation in the extracellular domain of MPZ,...
20.
Vital C, Gray F, Vital A, Ferrer X, Julien J
Clin Exp Pathol
. 1999 Sep;
47(3-4):153-9.
PMID: 10472735
Objective: About 8% of prion disease cases are familial and a few are due to an octapeptide repeat insertion (OPRI) in the prion protein gene. A suitable neuropathological examination has...