Derralynn Hughes - UCL | 人才画像

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论文共 468 篇作者统计合作学者相似作者

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The Development and Application of a Rapid and More Informative Test for Autoantibodies to Enzyme Replacement Therapies in Fabry Disease

Tomas Baldwin,Ivan Doykov,Hibba Kurdi,James Moon,Derralynn Hughes,Kevin Mills,Wendy E. Heywood

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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Twelve Years of the Gaucher Outcomes Survey (GOS): Insights, Achievements, and Lessons Learned from a Global Patient Registry

Deborah Elstein,Nadia Belmatoug,Bruno Bembi,Patrick Deegan,Diego Fernandez-Sasso,Pilar Giraldo,Ozlem Goker-Alpan,Derralynn Hughes,Heather Lau,Elena Lukina,Shoshana Revel-Vilk,Ida Vanessa D. Schwartz,Majdolen Istaiti,Jaco Botha,Noga Gadir,Joern Schenk,Ari Zimran

JOURNAL OF CLINICAL MEDICINEno. 12 (2024)

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Home-infusion Experience in Patients with Pompe Disease Receiving Avalglucosidase Alfa During Three Clinical Trials (COMET, NEO-EXT, and Mini-COMET)

Jordi Daz-Manera,Derralynn Hughes,Anthony Behin,Francoise Bouhour,James Davison,Sevim Erdem-Ozdamar,Si Houn Hahn,Kristina An Haack,Olivier Huynh-Ba,Magali Periquet,Swathi Tammireddy,Nathan Thibault,Tianyue Zhou,Celine Tard,Ans T. van der Ploeg

Molecular genetics and metabolism（2024）

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Expérience Des Patients Fabry Concernant La Perfusion Mensuelle De PegunigaLsidasE Alfa - Étude PEOPLE

François Eyskens, M. Ankit,Antonio Pisani,Ulla Feldt‐Rasmussen,Derralyn Hughes,Patrick Deegan, G.A. Ozlem,Eric Wallace,John Bernat,Nicola Longo, Francesco Bianchi,Rossana Rocco, Ylenia Paleari

La Revue de médecine interne (2024): A142-A143

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Transition of Patients with Gaucher Disease Type 1 from Pediatric to Adult Care: Results from Two International Surveys of Patients and Health Care Professionals

Karolina M. Stepien,Irena Znidar, Beata Kiec-Wilk, Angel Jones,Daniela Castillo-Garcia,Magy Abdelwahab,Shoshana Revel-Vilk, Ella Lineham,Derralynn Hughes,Uma Ramaswami,Tanya Collin-Histed

FRONTIERS IN PEDIATRICS (2024)

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Multiorgan Involvement in Females with Fabry Disease: Results from Two Phase III Trials and the Followme Registry

Peter Nordbeck,Derralynn A. Hughes,Albina Nowak,Robert J. Hopkin,Biliana O. Veleva-Rotse,Eva Krusinska,Ana Jovanovic

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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Fabry Patient's Experience of Pegunigalsidase Alfa Monthly Infusion: PEOPLE Study

Ankit Mehta,Francois J. Eyskens,Antonio Pisani,Ulla Feldt-Rasmussen,Derralynn Hughes,Patrick B. Deegan,Ozlem Goker-Alpan,Eric Wallace,John Bernat,Nicola Longo, Francesco Bianchi,Rossana Rocco, Ylenia Paleari

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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Changes in Angiogenesis and Bone Turnover Markers in Patients with Gaucher Disease Developing Osteonecrosis

Simona D'Amore, Kenneth Eric Poole,Uma Ramaswami,Derralynn Hughes,Kathleen Page,Antonio Giovanni Solimando,Angelo Vacca, Timothy Martin Cox,Patrick Deegan, MRC GAUCHERITE Consortium

Metabolitesno. 11 (2024)

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Long-Term Treatment of Gaucher Disease with Velaglucerase Alfa in ERT-Naïve Patients from the Gaucher Outcome Survey (GOS) Registry

Patrick Deegan,Heather Lau,Deborah Elstein,Diego Fernandez-Sasso,Pilar Giraldo,Derralynn Hughes,Ari Zimran,Majdolen Istaiti,Noga Gadir,Jaco Botha,Shoshana Revel-Vilk

JOURNAL OF CLINICAL MEDICINEno. 10 (2024)

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Tolerability of Pegunigalsidase Alfa Across the Clinical Program: Integrated Analysis of Infusion-Related Reactions by Dosing Regimens

Ankit Mehta,Eric Wallace,Ales Linhart,Derralynn Hughes,Nicola Longo,Camilla Tondel,Bojan Vujkovac,Rossana Rocco,Irene Koulinska,Raul Chertkoff,Sari Alon,Anat Sakov,John Bernat

Molecular Genetics and Metabolismno. 2 (2024): 107888-107888

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