Christel Tran

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 15

Top Topics

Peritoneal Dialysis

Systematic Review

Cognitive Impairment

Top Venues

Orphanet journal of rare diseases

Annals of clinical and translational neurology

Journal of inherited metabolic disease

This page only lists publications with an associated author ORCID identifier.

Publications

Aurel T Tankeu, Despina Christina Pavlidou, Andrea Superti-Furga, Karim Gariani, Christel Tran
Overweight and obesity in adult patients with phenylketonuria: a systematic review. Orphanet journal of rare diseases 18 (1) (2023)
Aurel T Tankeu, Despina Christina Pavlidou, Andrea Superti-Furga, Karim Gariani, Christel Tran
Overweight and obesity in adult patients with phenylketonuria: a systematic review. Orphanet journal of rare diseases 18 (1) (2023)
Aurel T Tankeu, Despina Christina Pavlidou, Andrea Superti-Furga, Karim Gariani, Christel Tran
Overweight and obesity in adult patients with phenylketonuria: a systematic review. Orphanet journal of rare diseases 18 (1) (2023)
Aurel T Tankeu, Mohammed Barigou, Rosette Pedro, Rita De Micheli, Alexandre Bodmer, Laurence Genton, Tinh-Hai Collet, Christel Tran
[Is ketogenic diet effective against cancer ?] Revue medicale suisse 19 (819) (2023)
Aurel T Tankeu, Despina Christina Pavlidou, Andrea Superti-Furga, Karim Gariani, Christel Tran
Overweight and obesity in adult patients with phenylketonuria: a systematic review. Orphanet journal of rare diseases 18 (1) (2023)
Markus Gschwind, Nuria Garcia Segarra, André Schaller, Ramona Bolognini, Jean-Marc Nuoffer, Raphael Hourez, Manuel Deprez, Benoit Lhermitte, Philippe Maeder, Christel Tran, Thierry Kuntzer
Early-onset leukoencephalomyelopathy due to a biallelic NDUFV1 variant in a mid-forties patient. Annals of clinical and translational neurology 9 (6) (2022)
Karim Gariani, Antoine Klauser, Maria Isabel Vargas, François Lazeyras, Christel Tran
New Insight in Hyperinsulinism/Hyperammonemia Syndrome by Magnetic Resonance Imaging and Spectroscopy. Brain sciences 12 (3) (2022)
Despina Christina Pavlidou, Geraldine Van Winckel, Christel Tran
When Simple Phlebotomy Is the Cure: Porphyria Cutanea Tarda. Journal of general internal medicine 37 (13) (2022)
Camille Kumps, Julien Stanovici, Emmelie Chaibi, Belinda Campos-Xavier, Despina Christina Pavlidou, Christel Tran
Black cartilage: Incidentally discovered articular ochronosis during arthroplasty. Journal of inherited metabolic disease 44 (6) (2021)
Jean-Marc Good, Isis Atallah, Mayté Castro Jimenez, David H Benninger, Thierry Kuntzer, Andrea Superti-Furga, Christel Tran
NGS-Based Diagnosis of Treatable Neurogenetic Disorders in Adults: Opportunities and Challenges. Genes 12 (5) (2021)
Beryl Royer-Bertrand, Katarina Cisarova, Florence Niel Bütschi, Giovanni Foletti, Vincent Guinchat, Christel Tran, Andrea Superti-Furga, Jean-Marc Good
CNOT2 haploinsufficiency in a 40-year-old man with intellectual disability, autism, and seizures. American journal of medical genetics. Part A 185 (8) (2021)
Brice Touilloux, Henri Lu, Belinda Campos-Xavier, Andrea Superti-Furga, Michael Hauschild, Thérèse Bouthors, Christel Tran
Elevated lactate in Mauriac syndrome: still a mystery. BMC endocrine disorders 21 (1) (2021)
Karim Gariani, Marina Nascimento, Andrea Superti-Furga, Christel Tran
Clouds over IMD? Perspectives for inherited metabolic diseases in adults from a retrospective cohort study in two Swiss adult metabolic clinics. Orphanet journal of rare diseases 15 (1) (2020)
Béryl Royer-Bertrand, Pinelopi Tsouni, Patrick Mullen, Belinda Campos Xavier, Lauréane Mittaz Crettol, Alexander J Lobrinus, Joseph Ghika, Matthias R Baumgartner, Carlo Rivolta, Andrea Superti-Furga, Thierry Kuntzer, Christopher Francklyn, Christel Tran
Peripheral neuropathy and cognitive impairment associated with a novel monoallelic HARS variant. Annals of clinical and translational neurology 6 (6) (2019)
Camelia Voinea, Elena Gonzalez Rodriguez, Catherine Beigelman-Aubry, Victor Leroy, Bérengère Aubry-Rozier, Belinda Campos-Xavier, Diana Ballhausen, Romain Lazor, Frédéric Barbey, Luisa Bonafé, Andrea Superti-Furga, Christel Tran
Hepatosplenomegaly, pneumopathy, bone changes and fronto-temporal dementia: Niemann-Pick type B and SQSTM1-associated Paget's disease in the same individual. Journal of bone and mineral metabolism 37 (2) (2018)