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Glucose variability in 6-12-month-old healthy infants.
Hauschild M, Monnard C, Eldridge AL, Antoniou MC, Bouthors T, Hansen E, Dwyer AA, Rytz A, Darimont C. Hauschild M, et al. Front Nutr. 2023 Jul 12;10:1128389. doi: 10.3389/fnut.2023.1128389. eCollection 2023. Front Nutr. 2023. PMID: 37502727 Free PMC article.
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.
Villanueva C, Jacobson-Dickman E, Xu C, Manouvrier S, Dwyer AA, Sykiotis GP, Beenken A, Liu Y, Tommiska J, Hu Y, Tiosano D, Gerard M, Leger J, Drouin-Garraud V, Lefebvre H, Polak M, Carel JC, Phan-Hug F, Hauschild M, Plummer L, Rey JP, Raivio T, Bouloux P, Sidis Y, Mohammadi M, de Roux N, Pitteloud N. Villanueva C, et al. Among authors: hauschild m. Genet Med. 2015 Aug;17(8):651-9. doi: 10.1038/gim.2014.166. Epub 2014 Nov 13. Genet Med. 2015. PMID: 25394172 Free PMC article.
TRANSITION IN ENDOCRINOLOGY: Hypogonadism in adolescence.
Dwyer AA, Phan-Hug F, Hauschild M, Elowe-Gruau E, Pitteloud N. Dwyer AA, et al. Among authors: hauschild m. Eur J Endocrinol. 2015 Jul;173(1):R15-24. doi: 10.1530/EJE-14-0947. Epub 2015 Feb 4. Eur J Endocrinol. 2015. PMID: 25653257 Review.
Natural history of growth hormone deficiency in a pediatric cohort.
Deillon E, Hauschild M, Faouzi M, Stoppa-Vaucher S, Elowe-Gruau E, Dwyer A, Theintz GE, Dubuis JM, Mullis PE, Pitteloud N, Phan-Hug F. Deillon E, et al. Among authors: hauschild m. Horm Res Paediatr. 2015;83(4):252-61. doi: 10.1159/000369392. Epub 2015 Feb 11. Horm Res Paediatr. 2015. PMID: 25676059 Free article.
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism.
COST Action BM1105; Badiu C, Bonomi M, Borshchevsky I, Cools M, Craen M, Ghervan C, Hauschild M, Hershkovitz E, Hrabovszky E, Juul A, Kim SH, Kumanov P, Lecumberri B, Lemos MC, Neocleous V, Niedziela M, Djurdjevic SP, Persani L, Phan-Hug F, Pignatelli D, Pitteloud N, Popovic V, Quinton R, Skordis N, Smith N, Stefanija MA, Xu C, Young J, Dwyer AA. COST Action BM1105, et al. Among authors: hauschild m. Orphanet J Rare Dis. 2017 Mar 20;12(1):57. doi: 10.1186/s13023-017-0608-2. Orphanet J Rare Dis. 2017. PMID: 28320476 Free PMC article.
Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.
Xu C, Cassatella D, van der Sloot AM, Quinton R, Hauschild M, De Geyter C, Flück C, Feller K, Bartholdi D, Nemeth A, Halperin I, Pekic Djurdjevic S, Maeder P, Papadakis G, Dwyer AA, Marino L, Favre L, Pignatelli D, Niederländer NJ, Acierno J, Pitteloud N. Xu C, et al. Among authors: hauschild m. Genet Med. 2018 Aug;20(8):872-881. doi: 10.1038/gim.2017.197. Epub 2017 Nov 16. Genet Med. 2018. PMID: 29144511 Free article.
Accuracy, satisfaction and usability of a flash glucose monitoring system among children and adolescents with type 1 diabetes attending a summer camp.
Hansen EA, Klee P, Dirlewanger M, Bouthors T, Elowe-Gruau E, Stoppa-Vaucher S, Phan-Hug F, Antoniou MC, Pasquier J, Dwyer AA, Pitteloud N, Hauschild M. Hansen EA, et al. Among authors: hauschild m. Pediatr Diabetes. 2018 Nov;19(7):1276-1284. doi: 10.1111/pedi.12723. Epub 2018 Jul 31. Pediatr Diabetes. 2018. PMID: 30014625 Clinical Trial.
A novel CHD7 mutation in an adolescent presenting with growth and pubertal delay.
Antoniou MC, Bouthors T, Xu C, Phan-Hug F, Elowe-Gruau E, Stoppa-Vaucher S, Sloot AV, Acierno J, Cassatella D, Richard C, Dwyer A, Pitteloud N, Hauschild M. Antoniou MC, et al. Among authors: hauschild m. Ann Pediatr Endocrinol Metab. 2019 Mar;24(1):49-54. doi: 10.6065/apem.2019.24.1.49. Epub 2019 Mar 31. Ann Pediatr Endocrinol Metab. 2019. PMID: 30943680 Free PMC article.
275 results