Hauschild M - Search Results

1

[Follow-up and management of children born small for gestational age a endocrine and metabolic aspects].

Elowe-Gruau E, Phan-Hug F, Stoppa-Vaucher S, Pitteloud N, Hauschild M. Elowe-Gruau E, et al. Among authors: hauschild m. Rev Med Suisse. 2014 Feb 19;10(418):424, 426-9. Rev Med Suisse. 2014. PMID: 24640277 French.

2

[Severe chronic anemia and endocrine disorders in children].

Hauschild M, Theintz G. Hauschild M, et al. Rev Med Suisse. 2007 Apr 18;3(107):988-91. Rev Med Suisse. 2007. PMID: 17526372 Review. French.

3

[Current and future care for diabetes in children: from insulin to immunotherapy].

Dirlewanger M, Hauschild M, Phan-Hug F, Schwitzgebel VM. Dirlewanger M, et al. Among authors: hauschild m. Rev Med Suisse. 2011 Feb 23;7(283):430-6. Rev Med Suisse. 2011. PMID: 21452510 French.

4

[Caring for patients with pediatric endocrinopathies and diabetes into adulthood: challenges of an often difficult transition].

Phan-Hug F, Hauschild M, Dwyer A, Pitteloud N. Phan-Hug F, et al. Among authors: hauschild m. Rev Med Suisse. 2012 Nov 14;8(362):2170-2, 2174. Rev Med Suisse. 2012. PMID: 23240318 French.

5

Diabetes and immune thrombocytopenic purpura: a new association with good response to anti-CD20 therapy.

von Laer Tschudin L, Schwitzgebel VM, von Scheven-Gête A, Blouin JL, Hofer M, Hauschild M, Ansari M, Stoppa-Vaucher S, Phan-Hug F. von Laer Tschudin L, et al. Among authors: hauschild m. Pediatr Diabetes. 2015 Mar;16(2):138-45. doi: 10.1111/pedi.12128. Epub 2014 Feb 19. Pediatr Diabetes. 2015. PMID: 24552605

6

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.

7

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.

8

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.

9

[Transition in diabetology].

Hauschild M, Elowe-Gruau E, Dwyer A, Aquarone MP, Unal S, Jornayvaz FR, Perrenoud L, Gastaldi G, Castellsague M, Dirlewanger M, Schwitzgebel VM. Hauschild M, et al. Rev Med Suisse. 2015 Feb 18;11(462):450-2, 454-5. Rev Med Suisse. 2015. PMID: 25915986 French.

10

DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.

Bouilly J, Messina A, Papadakis G, Cassatella D, Xu C, Acierno JS, Tata B, Sykiotis G, Santini S, Sidis Y, Elowe-Gruau E, Phan-Hug F, Hauschild M, Bouloux PM, Quinton R, Lang-Muritano M, Favre L, Marino L, Giacobini P, Dwyer AA, Niederländer NJ, Pitteloud N. Bouilly J, et al. Among authors: hauschild m. Hum Mol Genet. 2018 Jan 15;27(2):359-372. doi: 10.1093/hmg/ddx408. Hum Mol Genet. 2018. PMID: 29202173

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

282 results

Search Page

Filters