Zobrazeno 1 - 10
of 31
pro vyhledávání: '"R C, Reisin"'
Autor:
J E, de Sousa Santacreu, R C, Reisin, P, Bonardo, A, Carra, M M, Fernandez Pardal, G, Masenga, R, Torino, R V, Matera, M, Martinez
Publikováno v:
Revista de neurologia. 36(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51632f23866f2928c697b55409c8a868
https://pubmed.ncbi.nlm.nih.gov/12589610
https://pubmed.ncbi.nlm.nih.gov/12589610
Publikováno v:
Neurologia (Barcelona, Spain). 15(6)
Periodic paralysis is a well known complication of thytotoxicosis in Chinese and Japanese patients, but has been considered extremely rare in caucasians.Between 1991 and 1996, we admitted 8 caucasian patients to our Hospital due to thyrotoxic periodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d17f94eb64f6d07c2748093942788fa7
https://pubmed.ncbi.nlm.nih.gov/11002697
https://pubmed.ncbi.nlm.nih.gov/11002697
Publikováno v:
Musclenerve. 23(4)
In order to search for early changes induced by the application of human immunoglobulin G (IgG) on motor nerve terminals, IgG from patients with amyotrophic lateral sclerosis (ALS) and control subjects was injected subcutaneously into the levator aur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3272f149e3c5b4673cc15b57c38d88b3
https://pubmed.ncbi.nlm.nih.gov/10716765
https://pubmed.ncbi.nlm.nih.gov/10716765
Publikováno v:
Musclenerve. 19(5)
A 12-year-old developed a slowly progressive spastic gait at the age of 3. A marked loss of pain and temperature sensations led to a mutilating acropathy starting at age 5. Electrodiagnostic studies revealed a symmetric, axonal, predominantly sensory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abc3f5f37380aa452ac98fd191247090
https://pubmed.ncbi.nlm.nih.gov/8618564
https://pubmed.ncbi.nlm.nih.gov/8618564
Publikováno v:
Musclenerve. 16(12)
We identified 5 of 44 consecutive children (11%) with Guillain-Barré syndrome who had electrophysiologic evidence of severe reduction of the mean amplitude of the compound motor action potentials (mean CMAP amplitude10% of lower limit of normal). EM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3db946616810dd539ef85ac0eea6095
https://pubmed.ncbi.nlm.nih.gov/8232386
https://pubmed.ncbi.nlm.nih.gov/8232386
Publikováno v:
Journal of Clinical Neurophysiology. 5:200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd68d8c91c126d297a5630ad0bd6ebab
https://doi.org/10.1097/00004691-198804000-00035
https://doi.org/10.1097/00004691-198804000-00035
Autor:
Skedros, John G.1,2,3 jskedrosmd@uosmd.com, Phippen, Colton M.2 colronphipp@gmail.com, Langston, Tanner D.2 tannerlangston1@gmail.com, Mears, Chad S.2 chadmears330@gmail.com, Trujillo, Amy L.4 one2oneptpc@gmail.com, Miska, Robert M.5,6 robertmiska@gmail.com
Publikováno v:
Case Reports in Orthopedics. 8/12/2015, Vol. 2015, p1-6. 6p.
Autor:
Renard, Dimitri1 dimitrirenard@hotmail.com, Castelnovo, Giovanni1, Campello, Chantal1, Bouly, Stephane1, Le Floch, Anne1, Thouvenot, Eric1, Waconge, Anne1, Taieb, Guillaume1
Publikováno v:
Behavioural Neurology. 2014, p1-17. 17p.
Autor:
Bataveljic, Danijela1, Milosevic, Milena1, Radenovic, Lidija1 lidijar@bio.bg.ac.rs, Andjus, Pavle1
Publikováno v:
BioMed Research International. 2014, Vol. 2014, p1-7. 7p.
Publikováno v:
Current Medical Literature: Lysosomal Storage Disease. 2012, Vol. 10 Issue 1, p21-21. 1/4p.