Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rachel Harrison"'
Autor:
Ashely Wong, Caroline C. Davitt, Rachel Harrison, Colin Johnson, Anna Palatnik, Meredith Cruz
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 35:4478-4484
After failure of diet and exercise prescribed for gestational diabetes mellitus (GDM), pharmacotherapy initiation is recommended. The objective of this study was to examine the association between provider type and timing of pharmacotherapy initiatio
Autor:
Anand Velusamy, Angela F. Brady, Joseph Carlow, Huw Dorkins, Rebecca Igbokwe, Benjamin Whitelaw, Teng-Teng Chung, Rachel Harrison, Fiona Lalloo, Paul Brennan, Louise Izatt, Schaida Schirwani, Alan Kelsall, Barbara McGowan, Sophie T Williams, Rosemarie Davidson, Paul V. Carroll, Nicola Tufton, Patrick J. Morrison, Soo-Mi Park, Christopher Bowles, John Newell-Price, Julian Adlard, Monika Kosicka-Slawinska, Eamonn R. Maher, Richard M. Martin, Lara Hawkes, Rebecca Dyer, Scott Akker, Rupert Obholzer, Florian Wernig, Tricia Tan, Ruth T Casey, Prodromos Chatzikyriakou, Gemma White, Anna L. Mitchell, Mary Porteous
Publikováno v:
Clinical endocrinologyREFERENCES. 96(4)
Objective Phaeochromocytomas and paragangliomas (PPGL) are rare, but strongly heritable tumours. Variants in succinate dehydrogenase (SDH) subunits are identified in approximately 25% of cases. However, clinical and genetic information of patients wi
Autor:
Cyrus Cooper, Sujatha Gopal, Rebecca J Moon, Alan S. Rigby, Nicholas C. Harvey, Nick Bishop, Rachel Harrison
Publikováno v:
Bone Abstracts.
Publikováno v:
American Journal of Obstetrics and Gynecology. 222:S744
Publikováno v:
American Journal of Obstetrics and Gynecology. 222:S646
Autor:
Leslie G. Biesecker, William J. Rhead, Jennifer J. Johnston, Samantha A. Schrier Vergano, John M. Graham, Nancy Kramer, Bianca Russell, Benjamin M. Helm, Rachel Harrison, Amy Dobson, L. Kate Clarkson, Avi Z. Rosenberg, Catherine A. Brownstein, Angela Pickart, Wen-Hann Tan
Publikováno v:
American Journal of Medical Genetics Part A. 167:2122-2131
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual posture (flexion at the elbows with ulnar deviation, and flexion of the wri
Autor:
Vivek Dhir, Omar A. Abdul-Rahman, Nils Krone, Nicole Reisch, Laura G. Hendon, Hannah E Ivison, Rachel Harrison, Shelly Nielsen, Ann Haskins Olney, Beverly A. Hughes, Jan Idkowiak, Cedric H. L. Shackleton, Wiebke Arlt, Edward Blair
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
The Journal of Clinical Endocrinology & Metabolism; Vol 98
The Journal of Clinical Endocrinology & Metabolism; Vol 98
Context: Mutations in the electron donor enzyme P450 oxidoreductase (POR) result in congenital adrenal hyperplasia with apparent combined 17α-hydroxylase/17,20 lyase and 21-hydroxylase deficiencies, also termed P450 oxidoreductase deficiency (PORD).
Autor:
Abhijit Dixit, Sally A. Hulton, Nigel Smith, Chirag Patel, Rachel Harrison, Dominic J. McMullan, Lee Silcock, Mohnish Suri, Katherine Yates, Joanna Jarvis
Publikováno v:
American Journal of Medical Genetics Part A. :2317-2321
Deletions of 17q12 are associated with renal cysts and maturity onset diabetes of the young, and have also been identified in women with reproductive tract anomalies due to Mullerian aplasia. Although initially identified in patients with normal cogn
Publikováno v:
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Background For a patient with Hereditary Angioedema (HAE), physiological and/or psychological stress can cause insufficient control of local inflammatory pathways. This leads to complement and contact system activation and excess bradykinin resulting
Publikováno v:
Annals of Allergy, Asthma & Immunology. 115:77-78