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Tran, Christel
273  Ergebnisse:
Personensuche X
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1

Impact of genetic and non-genetic factors on phenotypic div..:

Hammann, Nicole ; Lenz, Dominic ; Baric, Ivo...
Molecular Genetics and Metabolism.  141 (2024)  3 - p. 108118 , 2024
Link: https://doi.org/10.1016/..
 
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2

Biotinidase deficiency: What have we learned in forty years:

Tankeu, Aurel T. ; Van Winckel, Geraldine ; Elmers, Jolanda...
Molecular Genetics and Metabolism.  138 (2023)  4 - p. 107560 , 2023
Link: https://doi.org/10.1016/..
 
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3

Overweight and obesity in adult patients with phenylketonur..:

Tankeu, Aurel T. ; Pavlidou, Despina Christina ; Superti-Furga, Andrea..
Orphanet Journal of Rare Diseases.  18 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

When Simple Phlebotomy Is the Cure: Porphyria Cutanea Tarda:

Pavlidou, Despina Christina ; Van Winckel, Geraldine ; Tran, Christel
Journal of General Internal Medicine.  37 (2022)  13 - p. 3489-3490 , 2022
Link: https://doi.org/10.1007/..
 
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5

Early‐onset leukoencephalomyelopathy due to a biallelic NDU..:

Gschwind, Markus ; Garcia Segarra, Nuria ; Schaller, André...
Annals of Clinical and Translational Neurology.  9 (2022)  6 - p. 888-892 , 2022
Link: https://doi.org/10.1002/..
 
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6

Fatigue chronique: quand suspecter une maladie héréditaired..:

Tankeu, Aurel T. ; Tran, Christel
Praxis.  111 (2022)  1 - p. 38-43 , 2022
Link: https://doi.org/10.1024/..
 
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7

New Insight in Hyperinsulinism/Hyperammonemia Syndrome by M..:

Gariani, Karim ; Klauser, Antoine ; Vargas, Maria Isabel..
Brain Sciences.  12 (2022)  3 - p. 389 , 2022
Link: https://doi.org/10.3390/..
 
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8

Partial lipodystrophy, severe dyslipidaemia and insulin res..:

Atallah, Isis ; McCormick, Dominique ; Good, Jean-Marc...
Journal of Clinical Lipidology.  16 (2022)  5 - p. 583-590 , 2022
Link: https://doi.org/10.1016/..
 
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9

Chronische Müdigkeit: Wann liegt der Verdacht auf eine erbl..:

Tankeu, Aurel T. ; Tran, Christel
Praxis.  111 (2022)  1 - p. 1-6 , 2022
Link: https://doi.org/10.1024/..
 
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10

Correction to: Elevated lactate in Mauriac syndrome: still ..:

Touilloux, Brice ; Lu, Henri ; Campos-Xavier, Belinda...
BMC Endocrine Disorders.  21 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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11

Black cartilage: Incidentally discovered articular ochronos..:

Kumps, Camille ; Stanovici, Julien ; Chaibi, Emmelie...
Journal of Inherited Metabolic Disease.  44 (2021)  6 - p. 1503-1504 , 2021
Link: https://doi.org/10.1002/..
 
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12

Elevated lactate in Mauriac syndrome: still a mystery:

Touilloux, Brice ; Lu, Henri ; Campos-Xavier, Belinda...
BMC Endocrine Disorders.  21 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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13

The fate of orally administered sialic acid: First insights..:

Tran, Christel ; Turolla, Licia ; Ballhausen, Diana...
Molecular Genetics and Metabolism Reports.  28 (2021)  - p. 100777 , 2021
Link: https://doi.org/10.1016/..
 
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14

Rhabdomyolyse d'effort:

DallAglio, Andrea ; Tran, Christel ; Jaccard, Evrim
Forum Médical Suisse ‒ Swiss Medical Forum.  , 2021
Link: https://doi.org/10.4414/..
 
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15

Spinal cerebrotendinous xanthomatosis: A case report and li..:

Atallah, Isis ; Millán, Diego San ; Benoît, Wicki...
Molecular Genetics and Metabolism Reports.  26 (2021)  - p. 100719 , 2021
Link: https://doi.org/10.1016/..
 
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