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Allan M. Lund

Rigshospitalet

46H指数
290论文数
7.6K被引数
收录论文 85
发表时间
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Phase 3 Randomized Trial Results of DTX401 AAV Gene Therapy for the Treatment of GSDIaDTX401 AAV基因疗法治疗GSDIa的III期随机试验结果
errJournal of Inherited Metabolic Disease
IF3.8
err2026-09-06
err0
errOAAI
errJohn J. Mitchell; Jose E. Abdenur; Foekje de Boer; Monica Boyer; Margo Sheck Breilyn; María-Luz Couce; Diva D. De Leon; Terry G. Derks; Areeg El-Gharbawy; Andrea B. Haijer-Schreuder; Karen Loechner; Nicola Longo; Allan M. Lund; Miguel Angel Martinez Olmos; Shawn E. McCandless; Bibiana Mello de Oliveira; Malaya Mount; Nicole Muschol; Kristina Pytlak; Kadakkal Radhakrishnan; Rebecca Riba-Wolman; David F. Rodriguez-Buritica; Alessandro La Rosa; Alessandro Rossi; Heather Saavedra; René Santer; Brian Shayota; G. Peter A. Smit; Carolina F. Moura De Souza; Melanie M. van der Klauw; David A. Weinstein; Joseph I. Wolfsdorf; Anne Blake; Andrew A. Grimm; Deepali Mitragotri; Syeda Rahman; Diane M. Turner-Bowker; Richard Collis
err分享
err收藏
Effect of long-term sepiapterin treatment on dietary phenylalanine tolerance in patients with phenylketonuria: interim results from the Phase 3 APHENITY Extension Study长期Sepiapterin治疗对苯丙酮尿症患者饮食苯丙氨酸耐受性的影响：APHENITY扩展研究III期研究的阶段性结果
errGenetics in Medicine
IF6.2
err2026-01-12
err0
errOAAI
errFrancjan van Spronsen; Heidi Peters; Lali Margvelashvili; Dodo Agladze; Ida Vanessa D. Schwartz; Maria Giżewska; Takashi Hamazaki; Laura Guilder; Anita MacDonald; Suresh Vijay; Anita Inwood; Maria Minami; Olivia Fjellbirkeland; Allan Lund; Melissa Lah; Janet A. Thomas; Nicola Longo; Ertuğrul Kiykim; Mika Ishige; Alberto Burlina
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Clinical assessment of growth patterns, weight, and dietary management in children and adults with phenylketonuria – a retrospective study苯丙酮尿症患者儿童与成人生长模式、体重及饮食管理的临床评估——一项回顾性研究
errOrphanet Journal of Rare Diseases
IF3.5
err2025-12-13
err0
errOAAI
errLionesa Bahtiri; Christine Jørgensen; Kirsten Ahring; Helle Rasmussen; Janne Meedon Hermansen; Olivia Welle Fjellbirkeland; Allan Meldgaard Lund; Mette Cathrine Ørngreen
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Nationwide study of the epidemiology and clinical features of X-linked adrenoleukodystrophy in Denmark全国性研究：丹麦X-连锁肾上腺脑白质营养不良的流行病学和临床特征
errMolecular Genetics and Metabolism
IF3.5
err2025-10-24
err0
errOAAI
errCecilie S. Videbæk; Morten Dunø; Suzanne G. Lindquist; Vibeke A. Larsen; Martin W. Kjær; Lars Melgaard; Jørgen E. Nielsen; Sabine W. Grønborg; Allan M. Lund
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Psychological Impact of Presymptomatic X-Linked ALD Diagnosis and Surveillance: A Small Qualitative Study of Patient and Parent Experiences无症状X-连锁肾上腺脑白质营养不良诊断与监测的心理影响：一项关于患者及家长经历的小型定性研究
errInternational Journal of Neonatal Screening 2024, Vol. 10, Page 73
IF4
err2025-08-21
err0
PREAI
errCecilie S. Videbæk; Sabine W. Grønborg; Allan M. Lund; Mette L. Olesen
err分享
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A diagnostic algorithm for inherited metabolic disorders using untargeted metabolomics一种用于遗传代谢病的非靶向代谢组学诊断算法
errMetabolomics
IF3.3
err2025-07-27
err0
errOAAI
errQian Gao; Adnan Khan; Mette Christensen; Xiaomin Zhou; Allan Lund; Sabine Weller Grønborg; Flemming Wibrand; Elsebet Østergaard; Thomas Moritz
err分享
err收藏
Outcome of Haemopoietic Stem Cell Transplantation in 21 Patients With Alpha-Mannosidosisα-甘露糖苷症21例患者的造血干细胞移植结局
errJournal of Inherited Metabolic Disease
IF3.8
err2025-06-23
err0
PREAI
errRobert Šáhó; Renata Formánková; Julie B. Eisengart; Allan Meldgaard Lund; Cecilie Videbaek; Berrak Bilginer Gürbüz; Namık Yaşar Özbek; Fatma Al Jasmi; Pavel Ješina
err分享
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Evolution of mobility, pain/discomfort, self-care, and mental health in patients with alpha-mannosidosis: an international caregiver and patient surveyα-甘露糖苷酶缺乏症患者移动能力、疼痛/不适、自我护理及心理健康的变化：一项国际照护者与患者调查
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2025-05-07
err0
errOAAI
errStepien, Karolina M.; Thomas, Sophie; Hennermann, Julia B.; Lampe, Christina; Muschol, Nicole M.; Ballesta-Martinez, Maria Juliana; Cruz, Jordi; Lopez-Rodriguez, Monica; Barth, Anneliese; Magner, Martin; Lund, Allan M.; Plaiasu, Vasilica; Ballabeni, Andrea; Dona, Francesca; Morgan, Heather M.; Guffon, Nathalie
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Long-term motor function and quality of life outcomes in patients with alpha-mannosidosis: Data from two velmanase alfa extension studies over 10 years
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2025-02-01
err0
PREAI
errGuffon, Nathalie; Borgwardt, Line; Tartaglione, Ester; Lund, Allan M.
err分享
err收藏
Outcome of hematopoietic stem cell transplantation in 19 patients with alpha-mannosidosis
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2025-02-01
err0
PREAI
errSaho, Robert; Formankova, Renata; Eisengart, Julie B.; Lund, Allan; Videbaek, Cecilie; Gurbuz, Berrak Bilginer; Ozbek, Namik Yasar; Al Jasmi, Fatma; Jesina, Pavel; Feillet, Francois; Pochon, Cecile; Guemann, Anne-Sophie; Alsayed, Moeen; Laktina, Sabine; Ucar, Sema Kalkan; Aksoylar, Serap; Lund, Troy; Orchard, Paul J.; Eminoglu, Fatma T.; Ileri, Talia; Kasapkara, cigdem S.; Yesilipek, Akif; Tuncel, Ali Tunc; Jurickova, Katarina; Magner, Martin
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Psychological Impact of Presymptomatic X-Linked ALD Diagnosis and Surveillance: A Small Qualitative Study of Patient and Parent Experiences
errINTERNATIONAL JOURNAL OF NEONATAL SCREENING
IF4
err2024-10-24
err0
errOAAI
errVidebaek, Cecilie S.; Gronborg, Sabine W.; Lund, Allan M.; Olesen, Mette L.
err分享
err收藏
Hematopoietic stem cell transplantation or enzyme replacement therapy in Gaucher disease type 3
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-08-01
err1
PREAI
errHoj, Astrid; Orngreen, Mette Cathrine; Naume, Marie Mostue; Lund, Allan Meldgaard
err分享
err收藏
Monitoring and integrated care coordination of patients with alpha-mannosidosis: A global Delphi consensus study
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-08-01
err1
errOAAI
errGuffon, Nathalie; Burton, Barbara K.; Ficicioglu, Can; Magner, Martin; Gil-Campos, Mercedes; Lopez-Rodriguez, Monica A.; Jayakar, Parul; Lund, Allan M.; Tal, Galit; Garcia-Ortiz, Jose Elias; Stepien, Karolina M.; Ellaway, Carolyn; Al-Hertani, Walla; Giugliani, Roberto; Cathey, Sara S.; Hennermann, Julia B.; Lampe, Christina; McNutt, Markey; Lagler, Florian B.; Scarpa, Maurizio; Sutton, V. Reid; Muschol, Nicole
err分享
err收藏
Late-Onset Molybdenum Cofactor Deficiency Type A: A Treatable Cause of Developmental Delay
errPEDIATRICS
IF6.4
err2024-05-29
err1
PREAI
errLund, Allan M.; Berland, Siren; Tangeraas, Trine; Christensen, Mette; Confer, Nils; Squires, Liza; Brannsether, Bente
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Efficacy and safety of oral sepiapterin in participants with phenylketonuria on sapropterin dihydrochloride at time of Phase 3 aphenity study entry
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-04-01
err0
PREAI
errZori, Roberto; Lah, Melissa; Offord, Staphanie; Lund, Allan; Opladen, Thomas; Peters, Heidi; Guilder, Laura; Ezgu, Faith; Breilyn, Margo Sheck; Manti, Filippo; Guerra, Ixiu del Carmen Cabrales; Ingalls, Kimberly; Zhao, Zhenming; Larkin, Alexandra; Hughes, Catalina; Somera-Molina, Kathleen; Smith, Neil; Longo, Nicola
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Preliminary results from the ongoing aphenity extension study: Sepiapterin reduces blood PHE with improved dietary PHE tolerance in participants with phenylketonuria
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-04-01
err0
PREAI
errSacharow, Stephanie; Muntau, Ania C.; Bratkovic, Drago; Margvelashvili, Lali; Agladze, Dodo; Guilder, Laura; Schwartz, Ida Vanessa D.; Minami, Maria Avanise Yumi; Kiykim, Ertugrul; Guerra, Ixiu del Carmen Cabrales; Zori, Roberto; Campistol, Jaume; Oliveira, Anabela; Janeiro, Patricia; Rutsch, Frank; Lund, Allan; Mungan, Halise; Vijay, Suresh; MacDonald, Anita; Chakrapani, Anupam; Opladen, Thomas; Tchan, Michel; Ingalls, Kimberly; Hughes, Catalina; Zhao, Zhenming; Larkin, Alexandra; Smith, Neil; Lah, Melissa
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Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia (vol 36, pg 1786, 2019)
errADVANCES IN THERAPY
IF4
err2024-02-20
err0
errOAAI
errBen-Omran, Tawfeg; Masana, Luis; Kolovou, Genovefa; Ariceta, Gema; Novoa, F. Javier; Lund, Allan M.; Bogsrud, Martin P.; Araujo, Maria; Hussein, Osamah; Ibarretxe, Daiana; Sanchez-Hernandez, Rosa M.; Santos, Raul D.
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err收藏
The investigation of the profiles of Lyso-Gb3 and related analogues in children with Fabry disease using tandem mass spectrometry
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-02-01
err0
PREAI
errEffraimidis, Grigorios; Auray-Blais, Christiane; Lavoie, Pamela; Lund, Allan; Feldt-Rasmussen, Ulla
err分享
err收藏
A Delphi consensus approach to monitoring and integrated care coordination of patients with alpha-mannosidosis
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-02-01
err0
PREAI
errMuschol, Nicole M.; Burton, Barbara K.; Ficicioglu, Can; Magner, Martin; Gil-Campos, Mercedes; Lopez-Rodriguez, Monica; Jayakar, Parul; Lund, Allan; Tal, Galit; Garcia, Jose E.; Stepien, Karolina M.; Ellaway, Carolyn; Al-Hertani, Walla; Giugliani, Roberto; Cathey, Sara; Hennermann, Julia B.; Lampe, Christina; McNutt, Markey; Lagler, Florian; Scarpa, Maurizio; Sutton, V. Reid; Guffon, Nathalie
err分享
err收藏
Long-term efficacy of velmanase alfa treatment in patients with alpha-mannosidosis: Pooled data from two extension studies (up to 12 years of therapy)
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2024-02-01
err1
PREAI
errGuffon, Nathalie; Borgwardt, Line; Tylki-Szymanska, Anna; Ballabeni, Andrea; Dona, Francesca; Joseph, Amer; Nienhuis, Henriet; Maugeri, Caterina; Lund, Allan
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研究方向

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合作学者
合作期刊
J
Jens J. Holst
H 指数: 193 · 论文数: 2.7K
R
Ronald J. A. Wanders
H 指数: 124 · 论文数: 1.1K
A
Anders Juul
H 指数: 106 · 论文数: 1.0K
G
Georg F. Hoffmann
H 指数: 101 · 论文数: 1.1K
V
Valérie Cormier‐Daire
H 指数: 99 · 论文数: 1.2K
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