Kết quả tìm kiếm - Vivek Dhir
- Đang hiển thị 1 - 12 kết quả của 12
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1
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency Bằng Nils Krone, Vivek Dhir, Hannah E Ivison, Wiebke Arlt
Được phát hành 2006Revisão -
2
A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency Bằng Jan Idkowiak, Tabitha Randell, Vivek Dhir, Pushpa Patel, Cedric Shackleton, Norman Taylor, Nils Krone, Wiebke Arlt
Được phát hành 2011Artigo -
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4
Premature adrenarche: novel lessons from early onset androgen excess Bằng Jan Idkowiak, Gareth G. Lavery, Vivek Dhir, Timothy Barrett, Paul M. Stewart, Nils Krone, Wiebke Arlt
Được phát hành 2011Revisão -
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A Novel Entity of Clinically Isolated Adrenal Insufficiency Caused by a Partially Inactivating Mutation of the Gene Encoding for P450 Side Chain Cleavage Enzyme (CYP11A1) Bằng Silvia Parajes, Clemens Kamrath, Ian T. Rose, Angela E. Taylor, Christiaan F. Mooij, Vivek Dhir, Joachim Grötzinger, Wiebke Arlt, Nils Krone
Được phát hành 2011Artigo -
7
Alternative pathway androgen biosynthesis and human fetal female virilization Bằng Nicole Reisch, Angela E. Taylor, Edson Nogueira, Daniel J. Asby, Vivek Dhir, Andrew Berry, Nils Krone, Richard J. Auchus, Cedric Shackleton, Neil A. Hanley, Wiebke Arlt
Được phát hành 2019Artigo -
8
Inactivating<i>PAPSS2</i>Mutations in a Patient with Premature Pubarche Bằng C. Noordam, Vivek Dhir, Joanne McNelis, Florian Schlereth, Neil A. Hanley, Nils Krone, Jan Smeitink, Roel Smeets, Fred C.G.J. Sweep, Hedi L. Claahsen‐van der Grinten, Wiebke Arlt
Được phát hành 2009Artigo -
9
Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency Bằng Nicole Reisch, Jan Idkowiak, Beverly Hughes, Hannah E Ivison, Omar Abdul‐Rahman, Laura G. Hendon, Ann Haskins Olney, Shelly Nielsen, Rachel Harrison, Edward Blair, Vivek Dhir, Nils Krone, Cedric Shackleton, Wiebke Arlt
Được phát hành 2013Artigo -
10
SIMBA: Online Simulation for Teaching Medical Cases to Preclinical Students—A Pilot Study Bằng Aditya Swaminathan, Dengyi Zhou, Isabel Allison, Tamzin Ogiliev, Fatema Rezai, Georgia Morgan, Haaziq Sheikh, Farah Abdelhameed, Harjeet Kaur, Alice Yip, Catherine Cooper, Meri Davitadze, Eka Melson, Paul Foster, Vivek Dhir, Punith Kempegowda
Được phát hành 2025Artigo -
11
Functional Consequences of Seven Novel Mutations in the<i>CYP11B1</i>Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency Bằng Silvia Parajes, Lourdes Loidi, Nicole Reisch, Vivek Dhir, Ian T. Rose, Rainer Hampel, Marcus Quinkler, Gerard S. Conway, Lidia Castro-Feijóo, David Araújo‐Vilar, Manuel Pombo, Fernando Domı́nguez, Emma L. Williams, Trevor Cole, Jeremy Kirk, Elke Kaminsky, Gill Rumsby, Wiebke Arlt, Nils Krone
Được phát hành 2010Artigo -
12
Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency Bằng Nils Krone, Nicole Reisch, Jan Idkowiak, Vivek Dhir, Hannah E Ivison, Beverly Hughes, Ian T. Rose, Donna O’Neil, Raymon Vijzelaar, Matthew J. Smith, Fiona MacDonald, Trevor Cole, Nicolai Adolphs, John Barton, Edward Blair, Stephen R. Braddock, Felicity Collins, Deborah Cragun, Mehul Dattani, Ruth Day, Shelley Dougan, Miriam Feist, Michael Gottschalk, John W. Gregory, Michaela Haim, Rachel Harrison, Ann Haskins Olney, Berthold P. Hauffa, Peter C. Hindmarsh, Robert J. Hopkin, Petr Jira, Marlies Kempers, Michiel N. Kerstens, Mohamed M. Khalifa, Birgit Köhler, Dominique Maiter, Shelly Nielsen, Stephen O’Riordan, Christian Roth, Kate Shane-Carson, Martin Silink, Nike Stikkelbroeck, Elizabeth Sweeney, Maria Szarras‐Czapnik, John Waterson, Lori Williamson, Michaela F. Hartmann, Norman Taylor, Stefan A. Wudy, E Małunowicz, Cedric Shackleton, Wiebke Arlt
Được phát hành 2011Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Internal medicine
Medicine
Endocrinology
Biology
Hormone
Gene
Genetics
Insulin resistance
Polycystic ovary
Androgen
Androgen Excess
Congenital adrenal hyperplasia
Biochemistry
Enzyme
Insulin
Mutation
Steroid
21-Hydroxylase
Adrenarche
Compound heterozygosity
Missense mutation
Phenotype
Steroid 11-beta-hydroxylase
Virilization
Adrenal insufficiency
CYP17A1
Dehydroepiandrosterone
Dehydroepiandrosterone sulfate
Fetus
Genotype