François Maillot - University Hospital Internal Medicine

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论文共 356 篇作者统计合作学者相似作者

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Trismus as a new feature of VEXAS syndrome

Alexis Archambeaud, Claire Le Dreau,Adrien Bigot,Olivier Kosmider, Assia Taleb, Lara Boucher,Marie Temple,Jean-Philippe Cottier,François Maillot, Alexandra Audemard-Verger

Rheumatology (Oxford, England) (2024)

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Episodic memory and speed of processing: Influence of plasma phenylalanine concentration in adults with early-treated phenylketonuria

Maxime Brachet,Sybil Charriere,Francois Maillot,Francois Feillet,Alain Fouilhoux,Leonardo Astudillo,Christian Lavigne,Jean Baptiste Arnoux,Sylvie Odent,Claire Gay,Manuel Schiff, Karin Mazodier,

Molecular Genetics and Metabolismno. 4 (2024): 108307

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Pegtibatinase, an investigational enzyme replacement therapy, for the treatment of classical homocystinuria (HCU): Design of the harmony Phase 3 study

Janet Thomas, Tawfeg Ben-Omran, Harvey Levy,Francois Maillot, Sharon McDermott, Sergio Slawka,Can Ficicioglu

Molecular Genetics and Metabolismno. 4 (2024): 108322

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Évaluation de la prévalence de l’hypersomnolence chez des patients adultes atteints de sclérose en plaques. Une étude observationnelle, transversale

Clémence Simonato, Aude Maurousset,Anne Marie Guennoc,Philippe Corcia, Marco Pasi,François Maillot,Nadège Limousin

Médecine du Sommeilno. 1 (2024): 33

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Homocysteine and methylmalonic acid in Phenylketonuria patients

Giovana Regina Weber Hoss,Fernanda Sperb-Ludwig,Tássia Tonon,Soraia Poloni, Sidney Behringer,Henk J. Blom,François Maillot,Ida Vanessa Doederlein Schwartz

Genetics and Molecular Biology（2024）

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Blood cytopenias as manifestations of inherited metabolic diseases: a narrative review

Yannick Moutapam-Ngamby—Adriaansen,François Maillot,François Labarthe,Bertrand Lioger

Orphanet Journal of Rare Diseases（2024）

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Pegtibatinase, an investigational enzyme replacement therapy, for the treatment of classical homocystinuria (HCU): Design of the harmony Phase 3 study

Janet Thomas,Tawfeg Ben-Omran, Harvey Levy,Francois Maillot, Sharon McDermott, Sergio Slawka,Can Ficicioglu

Molecular Genetics and Metabolismno. 4 (2024)

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Management of phenylketonuria in European PKU centres remains heterogeneous

Ahring Kirsten,Belanger-Quintana Amaya,Burlina Alberto,Gizewska Maria,Maillot Francois,Muntau Ania, Roscher Anne,Macdonald Anita

MOLECULAR GENETICS AND METABOLISMno. 1 (2024): 108120-108120

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Long-term comparative effectiveness of pegvaliase versus medical nutrition therapy with and without sapropterin in adults with phenylketonuria

Barbara K. Burton, Gillian E. Clague,Cary O. Harding, Ece Kucuksayrac, Drew G. Levy,Kristin Lindstrom,Nicola Longo,Francois Maillot,Ania C. Muntau,Frank Rutsch,Roberto T. Zori

MOLECULAR GENETICS AND METABOLISMno. 1 (2024): 108114-108114

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Mass cytometry reveals atypical immune profile notably impaired maturation of memory CD4 T with Gb3-related CD27 expression in CD4 T cells in Fabry disease

Wladimir Mauhin, Gaelle Dzangue-Tchoupou,Damien Amelin,Aurélien Corneau,Foudil Lamari, Yves Allenbach,Bertrand Dussol,Vanessa Leguy-Seguin, Pauline D'Halluin,Marie Matignon,François Maillot, Kim-Heang Ly,

Journal of inherited metabolic disease (2024)

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