McElreavey K - Search Results

1

Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.

Seeherunvong T, Ukarapong S, McElreavey K, Berkovitz GD, Perera EM. Seeherunvong T, et al. Among authors: mcelreavey k. J Pediatr Endocrinol Metab. 2012;25(1-2):121-3. doi: 10.1515/jpem.2011.370. J Pediatr Endocrinol Metab. 2012. PMID: 22570960

2

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD. McElreavey K, et al. Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8590-4. doi: 10.1073/pnas.93.16.8590. Proc Natl Acad Sci U S A. 1996. PMID: 8710915 Free PMC article.

3

True hermaphroditism: clinical aspects and molecular studies in 16 cases.

Damiani D, Fellous M, McElreavey K, Barbaux S, Barreto ES, Dichtchekenian V, Setian N. Damiani D, et al. Among authors: mcelreavey k. Eur J Endocrinol. 1997 Feb;136(2):201-4. doi: 10.1530/eje.0.1360201. Eur J Endocrinol. 1997. PMID: 9116916

4

Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments.

Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N. Damiani D, et al. Among authors: mcelreavey k. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):827-31. doi: 10.1515/jpem.1999.12.6.827. J Pediatr Endocrinol Metab. 1999. PMID: 10614539

5

Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K. Ottolenghi C, et al. Among authors: mcelreavey k. J Clin Endocrinol Metab. 2001 Jun;86(6):2465-9. doi: 10.1210/jcem.86.6.7539. J Clin Endocrinol Metab. 2001. PMID: 11397841

6

Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature.

Ergun-Longmire B, Vinci G, Alonso L, Matthew S, Tansil S, Lin-Su K, McElreavey K, New MI. Ergun-Longmire B, et al. Among authors: mcelreavey k. J Pediatr Endocrinol Metab. 2005 Aug;18(8):739-48. doi: 10.1515/jpem.2005.18.8.739. J Pediatr Endocrinol Metab. 2005. PMID: 16200839

7

Early recognition of gonadal dysgenesis in congenital nephrotic syndrome .

Ukarapong S, Berkovitz G, McElreavey K, Bashamboo A, Bao Y. Ukarapong S, et al. Among authors: mcelreavey k. Clin Nephrol. 2016 Dec;86 (2016)(12):341-344. doi: 10.5414/CN108925. Clin Nephrol. 2016. PMID: 27719739

8

SRY-negative 46,XX testicular/ovotesticular DSD: Long-term outcomes and early blockade of gonadotropic axis.

Lambert S, Peycelon M, Samara-Boustani D, Hyon C, Dumeige L, Peuchmaur M, Fiot E, Léger J, Simon D, Paye-Jaouen A, Bouligand J, Siffroi JP, Carel JC, McElreavey K, El Ghoneimi A, Brachet C, Bouvattier C, Martinerie L. Lambert S, et al. Among authors: mcelreavey k. Clin Endocrinol (Oxf). 2021 Apr;94(4):667-676. doi: 10.1111/cen.14389. Epub 2020 Dec 26. Clin Endocrinol (Oxf). 2021. PMID: 33296530

9

Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family.

Alla A, Ongoth FEM, Tahiri A, Karrou M, Rouf S, Benhaddou H, Kamaoui I, Mcelreavey K, Latrech H. Alla A, et al. Among authors: mcelreavey k. J Pediatr Endocrinol Metab. 2022 Jun 6;35(9):1215-1221. doi: 10.1515/jpem-2021-0717. Print 2022 Sep 27. J Pediatr Endocrinol Metab. 2022. PMID: 35670320

10

Idiopathic male pseudohermaphroditism: variations in presentation and management.

Meau-Petit V, Marcou V, Trivin C, Lortat-Jacob S, McElreavey K, Brauner R. Meau-Petit V, et al. Among authors: mcelreavey k. J Pediatr Endocrinol Metab. 2005 Jun;18(6):569-75. doi: 10.1515/jpem.2005.18.6.569. J Pediatr Endocrinol Metab. 2005. PMID: 16042324

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