Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nahla Alshaikh"'
Autor:
Abdulaziz S. AlSaman, Fouad Al Ghamdi, Ahmed K. Bamaga, Nahla AlShaikh, Mohammed Al Muqbil, Osama Muthaffar, Fahad A. Bashiri, Baleegh Ali, Arzu Mulayim, Elena Heider, Abdullah A. Alshahrani, Mohammed A. Al Muhaizea
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Duchenne muscular dystrophy (DMD) is a rare neuromuscular disorder that is characterized by progressive muscle weakness, resulting in disability and premature death. Onset of symptoms typically occurs at 2–3 years of age, and disease progression is
Externí odkaz:
https://doaj.org/article/48f3a8dd2e8649f4b391f6da29efacd2
Autor:
Ahmed K. Bamaga, Fouad Alghamdi, Nahla Alshaikh, Waleed Altwaijri, Fahad A. Bashiri, Khalid Hundallah, Musaad Abukhaled, Osama Y. Muthaffar, Sameer Al-Mehmadi, Tahani Ahmed Jamaly, Mohammad A. Al-Muhaizea, Abdulaziz Al-Saman
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: The coronavirus disease 2019 (COVID-19) pandemic has caused overwhelming challenges in healthcare worldwide. During such an outbreak, some needs of high-risk groups who require regular follow-ups and long-term management are not met. The
Externí odkaz:
https://doaj.org/article/7afbdcab69a64029b4233f05a7e46459
Autor:
Nahla Alshaikh
Publikováno v:
Clinical laboratory. 68(8)
Protein S is a central regulator of coagulation as it critically participates in down-regulation of both extrinsic and intrinsic pathways of the coagulation cascade. In this review, we aim to provide an update on protein S and its anticoagulant funct
Autor:
Fouad, Alghamdi, Nahla, Alshaikh, Ahmed K, Bamaga, Fahad A, Bashiri, Khalid, Hundallah, Ali, Alshehri, Mohammad, Al-Muhaizea, Abdulaziz, Al-Saman
Publikováno v:
Neurosciences
Autor:
Fahad A. Bashiri, Khalid Hundullah, Ali Alshehri, Ahmed K Bamaga, Nahla Alshaikh, Abdulaziz Al-Saman, Fouad Al-Ghamdi, Mohammad A. Al-Muhaizea
Publikováno v:
Neurosciences
Coronavirus disease 2019 (COVID-19) is caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV2). The World Health Organization declared COVID-19 to be a global health emergency on January 30, 2020, and its rapid spread was decl
Autor:
Oliver Brandau, Omid Paknia, Anett Marais, Lia Abbasi Moheb, Makia J. Marafi, Peter Bauer, Nouriya Al-Sannaa, Arndt Rolfs, Seham Alameer, Fahad Al-Hakami, Nana-Maria Grüning, Zafer Yüksel, Nahla Alshaikh, Aida M. Bertoli-Avella, Fahd Al-Mulla, Jose Maria Garcia-Aznar
Publikováno v:
European Journal of Human Genetics. 26:592-598
Congenital neurological disorders are genetically highly heterogeneous. Rare forms of hereditary neurological disorders are still difficult to be adequately diagnosed. Pertinent studies, especially when reporting only single families, need independen
Autor:
Giacomo Brisca, John Vissing, Nicol C. Voermans, Nahla Alshaikh, Angela Berardinelli, Adele D'Amico, Jahannaz Dastgir, Angel Sanchez, Carsten G. Bönnemann, Elio Maccagnano, Jordi Díaz-Manera, Lorenzo Maggi, Robert Carlier, Enzo Ricci, Giorgio Tasca, Susana Quijano-Roy, Gianmichele Magnano, Volker Straub, Mauro Monforte, Bjarne Udd, Elena Pegoraro, Eugenio Mercuri, Jana Haberlová, Francesco Muntoni, Nicoline Løkken, Baziel G.M. van Engelen, Francina Munell, Claudio Semplicini, Anna Pichiecchio, Fabiana Fattori, Maggie C. Walter, Claudio Bruno, D. Vlodavets, Chiara Marini-Bettolo, Enrico Bertini
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry, 89, 72-77
Journal of Neurology, Neurosurgery, and Psychiatry, 89, 1, pp. 72-77
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Journal of Neurology, Neurosurgery, and Psychiatry, 89, 1, pp. 72-77
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
ObjectivesTo characterise the pattern and spectrum of involvement on muscle MRI in a large cohort of patients with sarcoglycanopathies, which are limb-girdle muscular dystrophies (LGMD2C–2F) caused by mutations in one of the four genes coding for m
Autor:
Adnan Y. Manzur, Andreas Brunklaus, Ros Quinlivan, Tracey Davis, Stephanie Robb, Anna Sarkozy, Pinki Munot, Francesco Muntoni, Nahla Alshaikh
Publikováno v:
Archives of Disease in Childhood. 101:957-961
AimAssessment of the efficacy of vitamin D replenishment and maintenance doses required to attain optimal levels in boys with Duchenne muscular dystrophy (DMD).Method25(OH)-vitamin D levels and concurrent vitamin D dosage were collected from retrospe
Publikováno v:
Muscle & Nerve. 54:422-426
INTRODUCTION: Electrodiagnostic examination is perceived as a painful examination. An accurate assessment of its discomfort would be valuable to children, their parents, and clinicians. METHODS: We performed a prospective study of pediatric patients
Autor:
Abdulaziz Al-Saman, Nahla Alshaikh
Publikováno v:
Pediatric Neurology. 48:363-366
Types III and IV spinal muscular atrophy represent a diagnostic challenge due to the great variability in their presentation. We report a series of eight patients with type III spinal muscular atrophy who were followed for a long time for possible mu