The variability of responses to growth hormone therapy in children with short stature

por Savage, Martin O., Bang, Peter
Publicado 2012

Editorial: Controversies in growth hormone treatment and diagnosis

por Rapaport, Robert, Savage, Martin O.
Publicado 2022

Pediatric Cushing's disease: Management Issues

por Savage, Martin O., Storr, Helen L.
Publicado 2012

GH Resistance Is a Component of Idiopathic Short Stature: Implications for rhGH Therapy

por Savage, Martin O., Storr, Helen L.
Publicado 2021

Growth failure: ‘idiopathic’ only after a detailed diagnostic evaluation

por Rapaport, Robert, Wit, Jan M, Savage, Martin O
Publicado 2021

Applying precision medicine to the diagnosis and management of endocrine disorders

por Bidlingmaier, Martin, Gleeson, Helena, Latronico, Ana-Claudia, Savage, Martin O
Publicado 2022

Late-Onset Isolated Growth Hormone Deficiency

por Samuels, Julie G, Chimatapu, Sri Nikhita, Savage, Martin O, Rapaport, Robert
Publicado 2023

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

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

Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy

por Wit, Jan M., Deeb, Asma, Bin-Abbas, Bassam, Al Mutair, Angham, Koledova, Ekaterina, Savage, Martin O.
Publicado 2019

Managing Paediatric Growth Disorders: Integrating Technology Into a Personalised Approach

por Child, Jenny, Davies, Christine, Frost, Katie, McDermid, Eleanor, Pidcock, Rachel, Weinman, John, Savage, Martin O.
Publicado 2020

Evaluating the sensitivity and specificity of the UK and Dutch growth referral criteria in predicting the diagnosis of pathological short stature

por White, Gemma, Cosier, Shakira, Andrews, Afiya, Martin, Lee, Willemsen, Ruben, Savage, Martin O, Storr, Helen L
Publicado 2022

The growth hormone–insulin-like growth factor-I axis in the diagnosis and treatment of growth disorders

por Blum, Werner F, Alherbish, Abdullah, Alsagheir, Afaf, El Awwa, Ahmed, Kaplan, Walid, Koledova, Ekaterina, Savage, Martin O
Publicado 2018

Adherence to r-hGH Therapy in Pediatric Growth Hormone Deficiency: Current Perspectives on How Patient-Generated Data Will Transform r-hGH Treatment Towards Integrated Care

por Savage, Martin O, Fernandez-Luque, Luis, Graham, Selina, van Dommelen, Paula, Araujo, Matheus, de Arriba, Antonio, Koledova, Ekaterina
Publicado 2022

GHR gene transcript heterogeneity may explain phenotypic variability in GHR pseudoexon (6Ψ) patients

por Chatterjee, Sumana, Cottrell, Emily, Rose, Stephen J, Mushtaq, Talat, Maharaj, Avinaash V, Williams, Jack, Savage, Martin O, Metherell, Louise A, Storr, Helen L
Publicado 2020

Digital Health for Supporting Precision Medicine in Pediatric Endocrine Disorders: Opportunities for Improved Patient Care

por Fernandez-Luque, Luis, Al Herbish, Abdullah, Al Shammari, Riyad, Argente, Jesús, Bin-Abbas, Bassam, Deeb, Asma, Dixon, David, Zary, Nabil, Koledova, Ekaterina, Savage, Martin O.
Publicado 2021

Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia

por Hasenmajer, Valeria, Ferrigno, Rosario, Minnetti, Marianna, Pellegrini, Bianca, Isidori, Andrea M., Lenzi, Andrea, Salerno, Mariacarolina, Cappa, Marco, Chan, Li, De Martino, Maria Cristina, Savage, Martin O.
Publicado 2023

Paediatric Cushing’s disease: Epidemiology, pathogenesis, clinical management and outcome

por Ferrigno, Rosario, Hasenmajer, Valeria, Caiulo, Silvana, Minnetti, Marianna, Mazzotta, Paola, Storr, Helen L, Isidori, Andrea M, Grossman, Ashley B, De Martino, Maria Cristina, Savage, Martin O
Publicado 2021

Diagnosis and management of growth disorders in Gulf Cooperation Council (GCC) countries: Current procedures and key recommendations for best practice

por Al Herbish, Abdullah S., Almutair, Angham, Bin Abbas, Bassam, Alsagheir, Afaf, Alqahtani, Mohammed, Kaplan, Walid, Deeb, Asma, El-Awwa, Ahmed, Al Khawari, Mona, Koledova, Ekaterina, Savage, Martin O.
Publicado 2016

Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid defi...

por Chan, Li F, Metherell, Louise A, Krude, Heiko, Ball, Colin, O'Riordan, Stephen M P, Costigan, Colm, Lynch, Sally A, Savage, Martin O, Cavarzere, Paolo, Clark, Adrian J L
Publicado 2009

Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

por Prasad, Rathi, Chan, Li F., Hughes, Claire R., Kaski, Juan P., Kowalczyk, Julia C., Savage, Martin O., Peters, Catherine J., Nathwani, Nisha, Clark, Adrian J. L., Storr, Helen L., Metherell, Louise A.
Publicado 2014