Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Christine M. Hall"'
Autor:
Ataf H. Sabir, Elizabeth Morley, Jameela Sheikh, Alistair D. Calder, Ana Beleza-Meireles, Moira S. Cheung, Alessandra Cocca, Mattias Jansson, Suzanne Lillis, Yogen Patel, Shu Yau, Christine M. Hall, Amaka C. Offiah, Melita Irving
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
Abstract Background Skeletal dysplasia (SD) conditions are rare genetic diseases of the skeleton, encompassing a heterogeneous group of over 400 disorders, and represent approximately 5% of all congenital anomalies. Developments in genetic and treatm
Externí odkaz:
https://doaj.org/article/2ba7db3ffb1d4355907a9d8ece8ef189
Autor:
Erin C. Tully, Christine M. Hall, Lee Branum-Martin, Lindsey L. Cohen, Emily G. Ronkin, Laura J. Dilly, Erin B. Tone
Publikováno v:
Autism : the international journal of research and practice. 26(5)
The Autism Diagnostic Observation Schedule, 2nd-edition (ADOS-2) Toddler Module is the current gold-standard measure of autism spectrum disorder (ASD), a neurodevelopmental condition more frequently diagnosed in toddler boys than girls. Some evidence
Autor:
Christine M Hall, Amaka C Offiah, Francesca Forzano, Mario Lituania, Gen Nishimura, Valerie Cormier-Daire
This atlas is intended to give obstetricians, paediatricians, neonatologists, radiologists, molecular and clinical geneticists and anatomo-pathologists, a thorough insight into conditions (and variants) of skeletal dysplasias. Clinical and imaging fi
Autor:
Eric M. Kanza, Amos Nyathirombo, Jemmah P. Larbelee, Nicholas O. Opoku, Didier K. Bakajika, Hayford M. Howard, Germain L. Mambandu, Maurice M. Nigo, Deogratias Ucima Wonyarossi, Françoise Ngave, Kambale Kasonia Kennedy, Kambale Kataliko, Kpehe M. Bolay, Simon K. Attah, George Olipoh, Sampson Asare, Mupenzi Mumbere, Michel Vaillant, Christine M. Halleux, Annette C. Kuesel
Publikováno v:
Parasites & Vectors, Vol 17, Iss 1, Pp 1-23 (2024)
Abstract Background After ivermectin became available, diethylcarbamazine (DEC) use was discontinued because of severe adverse reactions, including ocular reactions, in individuals with high Onchocerca volvulus microfilaridermia (microfilariae/mg ski
Externí odkaz:
https://doaj.org/article/4ceb592513504c51851aa39437b4b9bd
Autor:
Ataf H Sabir, Elizabeth Morley, Jameela Sheikh, Alistair D Calder, Ana Beleza-Meireles, Moira S Cheung, Alessandra Cocca, Mattias Jansson, Suzanne Lillis, Yogen Patel, Shu Yau, Christine M Hall, Amaka C Offiah, Melita Irving
BACKGROUNDSkeletal dysplasia (SD) conditions are rare genetic diseases of the skeleton, encompassing a heterogeneous group of over 400 disorders, and represent approximately 5% of all congenital anomalies. Developments in genetic and treatment techno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef8a2642989eb7a89a221d4fc79bc130
https://doi.org/10.21203/rs.3.rs-96770/v1
https://doi.org/10.21203/rs.3.rs-96770/v1
Publikováno v:
European journal of medical genetics. 64(3)
Three sibling fetuses identified with limb shortening and thoracic narrowing at twelve weeks’ gestation on first trimester ultrasound examination are presented. The parents were non-consanguineous, Caucasian, healthy, of normal stature and had a he
Publikováno v:
Rheumatology. 59
Background Hypophosphatasia (HPP) is a condition arising due to mutations in the gene encoding the tissue-non-specific alkaline phosphatase (TNSALP) isoenzyme (ALPL), leading to deficient activity of TNSALP. It can be inherited as an autosomal domina
Autor:
Brittany D.K. Gratreak, Alicia R. Sandoval, Kirsten D. Pickard, Swetha Atluri, Christine M. Hall
One year after the Supreme Court decision on Roe vs. Wade in 1973, the University of Arizona was awarded a bond through Senate Bill 1245 for renovations to its football stadium. However, it came at a high price that is still paid for by medical stude
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86d5a72a2c11e1b17baac7691b3b16d2
Publikováno v:
Journal of Hand Surgery (European Volume). 44:96-108
Thalidomide embryopathy results from the ingestion of thalidomide in the first trimester during pregnancy, causing multiple forms of congenital abnormalities of variable severity that involve all systems. The skeletal findings most frequently affect
Autor:
John M. Westfall, Angela Ortigoza Bonilla, María C. Lapadula, Paula L. Zingoni, William C. W. Wong, Knut A. Wensaas, Wilson D. Pace, Javier Silva-Valencia, Luciano F. Scattini, Amy P. P. Ng, Jo-Anne Manski-Nankervis, Zheng J. Ling, Zhuo Li, Adrian H. Heald, Adrian Laughlin, Robert S. Kristiansson, Christine M. Hallinan, Lay H. Goh, Gabriela Gaona, Signe Flottorp, Simon de Lusignan, María S. Cuba-Fuentes, Valborg Baste, Karen Tu, on behalf of INTRePID
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
ObjectivesThe majority of patients with respiratory illness are seen in primary care settings. Given COVID-19 is predominantly a respiratory illness, the INTernational ConsoRtium of Primary Care BIg Data Researchers (INTRePID), assessed the pandemic
Externí odkaz:
https://doaj.org/article/e1e1b60bc22b4aa1afe6d6797fa379eb