Heinrichs C - Search Results

1

Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature.

Verloes A, Elmer C, Lacombe D, Heinrichs C, Rebuffat E, Demarquez JL, Moncla A, Adam E. Verloes A, et al. Among authors: heinrichs c. Eur J Pediatr. 1993 Jan;152(1):75-7. doi: 10.1007/BF02072522. Eur J Pediatr. 1993. PMID: 8444212 Review.

2

Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review.

Vilain C, Mortier G, Van Vliet G, Dubourg C, Heinrichs C, de Silva D, Verloes A, Baumann C. Vilain C, et al. Among authors: heinrichs c. Am J Med Genet A. 2009 Jul;149A(7):1476-81. doi: 10.1002/ajmg.a.32678. Am J Med Genet A. 2009. PMID: 19504604 Free article. Review.

3

Children's virilization and the use of a testosterone gel by their fathers.

Brachet C, Vermeulen J, Heinrichs C. Brachet C, et al. Among authors: heinrichs c. Eur J Pediatr. 2005 Oct;164(10):646-7. doi: 10.1007/s00431-005-1714-z. Epub 2005 Jul 16. Eur J Pediatr. 2005. PMID: 16025298

4

Clinical, hormonal and imaging findings in 27 children with central diabetes insipidus.

De Buyst J, Massa G, Christophe C, Tenoutasse S, Heinrichs C. De Buyst J, et al. Among authors: heinrichs c. Eur J Pediatr. 2007 Jan;166(1):43-9. doi: 10.1007/s00431-006-0206-0. Epub 2006 Aug 31. Eur J Pediatr. 2007. PMID: 16944241

5

Delayed diagnosis of congenital hypopituitarism associated with low socio-economic status and/or migration.

Boros E, Casimir M, Heinrichs C, Brachet C. Boros E, et al. Among authors: heinrichs c. Eur J Pediatr. 2020 Jan;179(1):151-155. doi: 10.1007/s00431-019-03489-3. Epub 2019 Nov 6. Eur J Pediatr. 2020. PMID: 31691850

6

IGF1 haploinsufficiency in children with short stature: a case series.

Staels W, Alev N, Maystadt I, Chivu O, De Schepper J, Heinrichs C, Beckers D. Staels W, et al. Among authors: heinrichs c. Eur J Endocrinol. 2021 Jul 7;185(2):323-332. doi: 10.1530/EJE-20-1463. Eur J Endocrinol. 2021. PMID: 34125705

7

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

Sobrier ML, Netchine I, Heinrichs C, Thibaud N, Vié-Luton MP, Van Vliet G, Amselem S. Sobrier ML, et al. Among authors: heinrichs c. Hum Mutat. 2005 May;25(5):503. doi: 10.1002/humu.9332. Hum Mutat. 2005. PMID: 15841484

8

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.

Simonis N, Migeotte I, Lambert N, Perazzolo C, de Silva DC, Dimitrov B, Heinrichs C, Janssens S, Kerr B, Mortier G, Van Vliet G, Lepage P, Casimir G, Abramowicz M, Smits G, Vilain C. Simonis N, et al. Among authors: heinrichs c. J Med Genet. 2013 Sep;50(9):585-92. doi: 10.1136/jmedgenet-2013-101603. Epub 2013 Jun 28. J Med Genet. 2013. PMID: 23812909 Free PMC article.

9

Congenital Hypothyroidism: Long-Term Experience with Early and High Levothyroxine Dosage.

Uyttendaele M, Lambert S, Tenoutasse S, Boros E, Ziereisen F, Van Vliet G, Heinrichs C, Brachet C. Uyttendaele M, et al. Among authors: heinrichs c. Horm Res Paediatr. 2016;85(3):188-97. doi: 10.1159/000443958. Epub 2016 Feb 17. Horm Res Paediatr. 2016. PMID: 26881423

10

Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Diabetes Insipidus, and Cleft Palate in Mice and Men.

Brachet C, Kozhemyakina EA, Boros E, Heinrichs C, Balikova I, Soblet J, Smits G, Vilain C, Mathers PH. Brachet C, et al. Among authors: heinrichs c. J Clin Endocrinol Metab. 2019 Jul 1;104(7):2925-2930. doi: 10.1210/jc.2018-02316. J Clin Endocrinol Metab. 2019. PMID: 30811539 Free PMC article.

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