Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Stanley, Iyadurai"'
Autor:
Tina Eshaghian, Bahareh Rabbani, Reza Shervin Badv, Sahar Mikaeeli, Behdad Gharib, Stanley Iyadurai
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100553- (2023)
Externí odkaz:
https://doaj.org/article/58798953cb874275a9103a0b9a58b38a
Autor:
Rita Wyrebek, Mara DiBartolomeo, Sandra Brooks, Thomas Geller, Melissa Crenshaw, Stanley Iyadurai
Publikováno v:
Neuromuscular Disorders. 32:166-169
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::685b225f2c7167212e20e6a1413a8e76
https://doi.org/10.1016/j.nmd.2022.01.005
https://doi.org/10.1016/j.nmd.2022.01.005
Autor:
Stanley Iyadurai, Thomas Geller, Rita Wyrebek, Melissa Crenshaw, Sandra Brooks, Mara DiBartolomeo, Magdalena Mroczek
Publikováno v:
Neuromuscular Disorders.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a09866b3787871f79a5a28fc86e53cd
https://doi.org/10.1016/j.nmd.2022.11.001
https://doi.org/10.1016/j.nmd.2022.11.001
Autor:
Stanley Iyadurai
Publikováno v:
Neurologic Clinics. 38:541-552
Congenital myasthenic syndromes comprise a rare heterogeneous group of diseases that impair neuromuscular transmission and are characterized by muscle fatigability and transient or permanent weakness. Symptoms are often present from birth or early ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d88431d87d07f73dc0a6cd08c921c1f
https://doi.org/10.1016/j.ncl.2020.03.004
https://doi.org/10.1016/j.ncl.2020.03.004
Autor:
Silvia Bonanno, Riccardo Giossi, Riccardo Zanin, Valentina Porcelli, Claudio Iannacone, Giovanni Baranello, Gary Ingenito, Stanley Iyadurai, Zorica Stevic, Stojan Peric, Lorenzo Maggi
Publikováno v:
Journal of neurology. 269(11)
Spinal muscular atrophy (SMA) is an autosomal recessive disease where a deficient amount of SMN protein leads to progressive lower motor neuron degeneration. SMN-enhancing therapies are now available. Yet, fatigue and signs of impaired neuromuscular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37cabb275b2d4cfc0fa15a9ae2bb8b3a
https://pubmed.ncbi.nlm.nih.gov/35763114
https://pubmed.ncbi.nlm.nih.gov/35763114
Autor:
Raghav Govindarajan, Stanley Iyadurai, Alex Karenevich, Laura Herbelin, Jeffrey Statland, Richard Barohn
Publikováno v:
RRNMF Neuromuscular Journal. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed97379197e8f6b8429b8179adfaad77
https://doi.org/10.17161/rrnmf.v3i1.16747
https://doi.org/10.17161/rrnmf.v3i1.16747
Autor:
Swathi Beladakere Ramaswamy, John A Stanford, Stanley Iyadurai, Raghav Govindarajan, Richard Barohn
Publikováno v:
RRNMF Neuromuscular Journal. 3
Objective: To study the effect of 3,4-diaminopyridine phosphate (3,4-DAPP) on body weight, grip strength, neurological score and survival in symptomatic SOD1-G93A mice. Method: We administered 3,4-diaminopyridine phosphate (3,4-DAPP) at 0, 8, and 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ee3f9b22947521d04e3f889a815a87b
https://doi.org/10.17161/rrnmf.v2i5.15641
https://doi.org/10.17161/rrnmf.v2i5.15641
Autor:
Erwan Gasnier, David Vissiere, Laurent Servais, Tahseen Mozaffar, Gennyne Walker, Kathryn R. Wagner, John Vissing, Teresa Gidaro, M. Annoussamy, Sanjay S. Shukla, Stanley Iyadurai, Shahram Attarian
Publikováno v:
MusclenerveREFERENCES. 65(2)
INTRODUCTION/AIMS Limb girdle muscular dystrophy type 2B (LGMDR2) and facioscapulohumeral muscular dystrophy (FSHD) are genetic muscular dystrophies with an increasing number of potential therapeutic approaches. The aim of this study is to report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c297deefa536deb7b918d726a638be89
https://pubmed.ncbi.nlm.nih.gov/34687225
https://pubmed.ncbi.nlm.nih.gov/34687225
Autor:
Rita Wyrebek, Mara Di Bartolomeo, Sandra Brooks, Thomas Geller, Melissa Crenshaw, Stanley Iyadurai
Publikováno v:
Neuromuscular Disorders. 32:e1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbf24c5ec68fd1b232f7fb7c4e6d8172
https://doi.org/10.1016/j.nmd.2022.06.008
https://doi.org/10.1016/j.nmd.2022.06.008
Publikováno v:
Neuromuscular disorders : NMD. 31(7)
Andersen-Tawil syndrome is a rare, autosomal dominant, multisystem disorder for which the majority of cases are caused by pathogenic variants in the KCNJ2 gene. The syndrome is characterized by the clinical triad of episodic paralysis, cardiac conduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fb0abfdaafe947af902c41ea043269d
https://pubmed.ncbi.nlm.nih.gov/34078557
https://pubmed.ncbi.nlm.nih.gov/34078557