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Melissa Andrew
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Journal Articles

Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency

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Subject Area:
Karger e-Journal Backfile Collection 2023 , Endocrinology , Women's and Children's Health
Gajanthan Muthuvel, Andrew Dauber, Eirene Alexandrou, Leah Tyzinski, Melissa Andrew, Vivian Hwa, Philippe Backeljauw
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2023) 96 (5): 449–457.
https://doi.org/10.1159/000529071
Published Online: 16 January 2023
View articletitled, Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency
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Journal Articles

Targeted Searches of the Electronic Health Record and Genomics Identify an Etiology in Three Patients with Short Stature and High IGF-I Levels

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Subject Area:
Endocrinology , Women's and Children's Health
Catalina Cabrera-Salcedo, Colin P. Hawkes, Leah Tyzinski, Melissa Andrew, Guillaume Labilloy, Diego Campos, Amalia Feld, Annalisa Deodati, Vivian Hwa, Joel N. Hirschhorn, Adda Grimberg, Andrew Dauber, the Genomics Research and Innovation Network
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2020) 92 (3): 186–195.
https://doi.org/10.1159/000504884
Published Online: 13 February 2020
View articletitled, Targeted Searches of the Electronic Health Record and Genomics Identify an Etiology in Three Patients with Short Stature and High IGF-I Levels
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Journal Articles

Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia

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Subject Area:
Endocrinology , Women's and Children's Health
Christiaan de Bruin, Courtney Finlayson, Mariana F.A. Funari, Gabriela A. Vasques, Bruna Lucheze Freire, Antonio M. Lerario, Melissa Andrew, Vivian Hwa, Andrew Dauber, Alexander A.L. Jorge
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2016) 86 (5): 342–348.
https://doi.org/10.1159/000446476
Published Online: 02 June 2016
View articletitled, Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia
Open the PDF for Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia in another window
Journal Articles

Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 Deficiency

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Subject Area:
Endocrinology , Women's and Children's Health
Christiaan de Bruin, Zerrin Orbak, Melissa Andrew, Vivian Hwa, Andrew Dauber
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2016) 85 (5): 358–362.
https://doi.org/10.1159/000443684
Published Online: 21 January 2016
View articletitled, Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 Deficiency
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