STAT5B Deficiency: Impacts on Human Growth and Immunity

od Hwa, Vivian
Wydane w Growth Horm IGF Res (2015)

Human Growth Disorders Associated with Impaired GH action: Defects in STAT5B and JAK2

od Hwa, Vivian
Wydane w Mol Cell Endocrinol (2020)

Biology of the somatotroph axis (after the pituitary)

od Rosenfeld, Ron G., Hwa, Vivian
Wydane w Ann Endocrinol (Paris) (2017)

Novel Modulators of the Growth Hormone - Insulin-Like Growth Factor Axis: Pregnancy-Associated Plasma Protein-A2 and Stanniocalcin-2

od Fujimoto, Masanobu, Hwa, Vivian, Dauber, Andrew
Wydane w J Clin Res Pediatr Endocrinol (2017)

IGFBP-3 sensitizes prostate cancer cells to interferon-gamma-induced apoptosis

od Fang, Peng, Hwa, Vivian, Little, Brian M., Rosenfeld, Ron G.
Wydane 2007

Adrenal Insufficiency, Sex Reversal, and Angelman Syndrome due to Uniparental Disomy Unmasking a Mutation in CYP11A1

od Kim, Ahlee, Fujimoto, Masanobu, Hwa, Vivian, Backeljauw, Philippe, Dauber, Andrew
Wydane w Horm Res Paediatr (2018)

Severe short stature in two siblings as the presenting sign of ACP5 deficiency

od de Bruin, Christiaan, Orbak, Zerrin, Andrew, Melissa, Hwa, Vivian, Dauber, Andrew
Wydane w Horm Res Paediatr (2016)

Two Siblings with a Mutation in CCDC8 Presenting with Mild Short Stature: A Case of 3-M Syndrome

od Liao, Lihong, Gan, Hoong-Wei, Hwa, Vivian, Dattani, Mehul, Dauber, Andrew
Wydane w Horm Res Paediatr (2017)

PAPPA2 as a Therapeutic Modulator of IGF-I Bioavailability: in Vivo and in Vitro Evidence

od Andrew, Melissa, Liao, Lihong, Fujimoto, Masanobu, Khoury, Jane, Hwa, Vivian, Dauber, Andrew
Wydane w J Endocr Soc (2018)

A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent

od Poyrazoğlu, Şükran, Hwa, Vivian, Baş, Firdevs, Dauber, Andrew, Rosenfeld, Ron, Darendeliler, Feyza
Wydane w J Clin Res Pediatr Endocrinol (2019)

Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding protein

od Rughani, Ankur, Zhang, Dongsheng, Vairamani, Kanimozhi, Dauber, Andrew, Hwa, Vivian, Krishnan, Sowmya
Wydane w Clin Endocrinol (Oxf) (2020)

Genetic Defects in the Growth Hormone–IGF-I Axis Causing Growth Hormone Insensitivity and Impaired Linear Growth

od Savage, Martin O., Hwa, Vivian, David, Alessia, Rosenfeld, Ron G., Metherell, Louise A.
Wydane 2011

Severe Growth Deficiency is Associated with STAT5b Mutations that Disrupt Protein Folding and Activity

od Varco-Merth, Benjamin, Feigerlová, Eva, Shinde, Ujwal, Rosenfeld, Ron G., Hwa, Vivian, Rotwein, Peter
Wydane 2013

Genetic Causes of Growth Hormone Insensitivity beyond GHR

od Hwa, Vivian, Fujimoto, Masanobu, Zhu, Gaohui, Gao, Wen, Foley, Corinne, Kumbaji, Meenasri, Rosenfeld, Ron G
Wydane w Rev Endocr Metab Disord (2020)

Familial Short Stature Caused by Haploinsufficiency of The Insulin-like Growth Factor 1 Receptor Due to Nonsense-Mediated mRNA Decay

od Fang, Peng, Schwartz, I. David, Johnson, Betty D., Derr, Michael A., Roberts, Charles T., Hwa, Vivian, Rosenfeld, Ron G.
Wydane w Mol Endocrinol (2009)

Isolated Growth Hormone Deficiency due to the R183H Mutation in GH1: Clinical Analysis of a Four-Generation Family

od Cabrera-Salcedo, Catalina, Shah, Amy S., Andrew, Melissa, Tyzinski, Leah, Hwa, Vivian, Gutmark-Little, Iris, Backeljauw, Philippe, Dauber, Andrew
Wydane w Clin Endocrinol (Oxf) (2017)

OR07-5 A Cross-Sectional Study of IGF-I Bioavailability through Childhood: Associations with PAPP-A2 and Anthropometric Data

od Fujimoto, Masanobu, Khoury, Jane, Khoury, Philip, Kalra, Bhanu, Kumar, Ajay, Sluss, Patrick, Oxvig, Claus, Hwa, Vivian, Dauber, Andrew
Wydane w J Endocr Soc (2019)

OR07-6 Integrating Targeted Bioinformatic Searches of the Electronic Health Records and Genomic Testing Identifies a Molecular Diagnosis in Three Patients with Undiagnosed Short St...

od Cabrera Salcedo, Catalina, Labilloy, Guillaume, Andrew, Shayne, Hwa, Vivian, Tyzinski, Leah, Grimberg, Adda, Hawkes, Colin, Hirschhorn, Joel, Dauber, Andrew
Wydane w J Endocr Soc (2019)

A Novel ERCC6 Splicing Variant Associated with a Mild Cockayne Syndrome Phenotype

od Swartz, Jonathan M, Akinci, Aysehan, Andrew, Shayne F., Siğirci, Ahmet, Hirschhorn, Joel N, Rosenfeld, Ron G, Dauber, Andrew, Hwa, Vivian
Wydane w Horm Res Paediatr (2014)

Anthropometric and biochemical correlates of PAPP-A2, free IGF-I, and IGFBP-3 in childhood

od Fujimoto, Masanobu, Khoury, Jane C, Khoury, Philip R, Kalra, Bhanu, Kumar, Ajay, Sluss, Patrick, Oxvig, Claus, Hwa, Vivian, Dauber, Andrew
Wydane w Eur J Endocrinol (2020)