Tauber M - Search Results

1

Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype.

Chassaing N, De Mas P, Tauber M, Vincent MC, Julia S, Bourrouillou G, Calvas P, Bieth E. Chassaing N, et al. Among authors: tauber m. Am J Med Genet A. 2004 Aug 1;128A(4):410-3. doi: 10.1002/ajmg.a.30199. Am J Med Genet A. 2004. PMID: 15264288

2

Recurrent ovarian cyst and mutation of the Gs alpha gene in ovarian cyst fluid cells: what is the link with McCune-Albright syndrome?

Pienkowski C, Lumbroso S, Bieth E, Sultan C, Rochiccioli P, Tauber M. Pienkowski C, et al. Among authors: tauber m. Acta Paediatr. 1997 Sep;86(9):1019-21. doi: 10.1111/j.1651-2227.1997.tb15194.x. Acta Paediatr. 1997. PMID: 9343290

3

A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndrome.

Boulard S, Diene G, Barat R, Oliver I, Pienkowski C, Lacombe D, Vincent MC, Bourrouillou G, Tauber M. Boulard S, et al. Among authors: tauber m. Genet Couns. 2006;17(2):173-83. Genet Couns. 2006. PMID: 16970035 Review.

4

Human growth hormone receptor: cloning and expression of the full-length complementary DNA after site-directed inactivation of a cryptic bacterial promoter.

Bieth E, Cahoreau C, Cholin S, Molinas C, Cerutti, Rochiccioli P, Devauchelle G, Tauber M. Bieth E, et al. Among authors: tauber m. Gene. 1997 Jul 18;194(1):97-105. doi: 10.1016/s0378-1119(97)00173-x. Gene. 1997. PMID: 9266678

5

Evaluation of cutaneous modifications in seventy-seven growth hormone-deficient children.

Conte F, Diridollou S, Jouret B, Turlier V, Charveron M, Gall Y, Rochiccioli P, Bieth E, Tauber M. Conte F, et al. Among authors: tauber m. Horm Res. 2000;54(2):92-7. doi: 10.1159/000053238. Horm Res. 2000. PMID: 11251373

6

Heterozygous mutation in the WSXWS equivalaent motif of the growth hormone receptor in a child with poor response to growth hormone therapy.

Tauber MT, Porra V, Dastot F, Molinas C, Amselem S, Cholin S, Rochiccioli P, Bieth E. Tauber MT, et al. Growth Horm IGF Res. 1998 Jun;8(3):211-6. doi: 10.1016/s1096-6374(98)80113-5. Growth Horm IGF Res. 1998. PMID: 10984309

7

Growth hormone, insulin-like growth factor-I and insulin-like growth factor binding protein-3 are regulated differently in small-for-gestational-age and appropriate-for-gestational-age neonates.

Cance-Rouzaud A, Laborie S, Bieth E, Tricoire J, Rolland M, Grandjean H, Rochiccioli P, Tauber M. Cance-Rouzaud A, et al. Among authors: tauber m. Biol Neonate. 1998;73(6):347-55. doi: 10.1159/000013996. Biol Neonate. 1998. PMID: 9618051

8

Expression of a recombinant human growth hormone binding protein in baculovirus/insect cell system.

Cholin S, Bieth E, Molinas C, Cahoreau C, Perals C, Cerruti M, Devauchelle G, Rochiccioli P, Tauber M. Cholin S, et al. Among authors: tauber m. Biochimie. 1996;78(10):882-6. doi: 10.1016/s0300-9084(97)84342-8. Biochimie. 1996. PMID: 9116059

9

[3D echocardiography of the ascending aorta in Marfan's syndrome].

Dulac Y, Taktak A, Acar P, Abadir S, Chilon T, Edouard T, Julia S, Tauber M, Hovnanian A. Dulac Y, et al. Among authors: tauber m. Arch Mal Coeur Vaiss. 2005 May;98(5):538-41. Arch Mal Coeur Vaiss. 2005. PMID: 15966605 Clinical Trial. French.

10

Hypophosphatasia may lead to bone fragility: don't miss it.

Moulin P, Vaysse F, Bieth E, Mornet E, Gennero I, Dalicieux-Laurencin S, Baunin C, Tauber MT, De Gauzy JS, Salles JP. Moulin P, et al. Eur J Pediatr. 2009 Jul;168(7):783-8. doi: 10.1007/s00431-008-0835-6. Epub 2008 Sep 26. Eur J Pediatr. 2009. PMID: 18818947

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