Results 261 to 270 of about 6,845,162 (410)

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao, Katherine R Schon, Jana Vandrovcova, Özlem Yayıcı Köken, Sharika Raga, Kireshnee Naidu, Maryke Schoonen, Nimita Rani, Pedro Tomaselli, Dipti Baskar, Musambo Kapapa, Ipek Polat, Lindsay A Wilson, Kumarasamy Thangaraj, Uluç Yiş, Bevinahalli N Nandeesh, David Bearden, Michelle Kvalsund, Franclo Henning, Seena Vengalil, Atchayaram Nalini, Claudia F. R. Sobreira, Wilson Marques, Haluk Topoloğlu, Michael G Hanna, Sireesha Yareeda, Venugopalan Y Vishnu, Francois H van der Westhuizen, Izelle Smuts, Surita Meldau, Jo Wilmshurst, Büşranur Çavdarlı, Jeannine Heckmann, Patrick F Chinnery, Rita Horvath   +34 more
wiley   +1 more source

Assessing the value of health information exchange organizations to hospital interoperability. [PDF]

Health Aff Sch
Richwine C, Strawley C, Chang W, Everson J.   +3 more
europepmc   +1 more source

'A tough nut to crack': inconsistent standards as roadblocks to data interoperability of health information systems in public hospitals in the Gauteng Province of South Africa. [PDF]

Oxf Open Digit Health
Chuma KG.
europepmc   +1 more source

Clinical Lectures in Course of Delivery during the Present Session, at Guy's Hospital [PDF]

B. B. Cooper
openalex   +1 more source

Why Patients Go to Hospital [PDF]

, 1959
John Fry
openalex   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala   +17 more
wiley   +1 more source

Hospital governance accountability challenges in Iran: a qualitative study. [PDF]

BMC Health Serv Res
Jalilvand MA, Raeisi AR, Shaarbafchizadeh N.   +2 more
europepmc   +1 more source

Hospitality

, 2014
openaire   +2 more sources

Strategies to Prevent Central Line–Associated Bloodstream Infections in Acute Care Hospitals: 2014 Update

Infection Control & Hospital Epidemiology, 2014
J. Marschall, L. Mermel, M. Fakih, L. Hadaway, A. Kallen, N. O’grady, A. M. Pettis, M. Rupp, Thomas J. Sandora, L. Maragakis, D. Yokoe   +10 more
semanticscholar   +1 more source

A Clinical Lecture on the Rhinoplastic Operation: Delivered in the Meath Hospital and Co. Dublin Infirmary [PDF]

, 1899
William Stokes
openalex   +1 more source