Baron S - Search Results

1

46,XY pure gonadal dysgenesis: clinical presentations and management of the tumor risk.

Capito C, Leclair MD, Arnaud A, David A, Baron S, Corradini N, Héloury Y. Capito C, et al. Among authors: baron s. J Pediatr Urol. 2011 Feb;7(1):72-5. doi: 10.1016/j.jpurol.2010.01.010. Epub 2010 Feb 11. J Pediatr Urol. 2011. PMID: 20153258

2

[Precocious puberty in children adopted from foreign countries].

Baron S, Battin J, David A, Limal JM. Baron S, et al. Arch Pediatr. 2000 Aug;7(8):809-16. doi: 10.1016/s0929-693x(00)80189-x. Arch Pediatr. 2000. PMID: 10985180 French.

3

46,XY gonadal dysgenesis: evidence for autosomal dominant transmission in a large kindred.

Le Caignec C, Baron S, McElreavey K, Joubert M, Rival JM, Mechinaud F, David A. Le Caignec C, et al. Among authors: baron s. Am J Med Genet A. 2003 Jan 1;116A(1):37-43. doi: 10.1002/ajmg.a.10820. Am J Med Genet A. 2003. PMID: 12476449

4

Cone-rod dystrophy, growth hormone deficiency and spondyloepiphyseal dysplasia: report of a new case without nephronophtisis.

Isidor B, Le Merrer M, Ramos E, Baron S, David A. Isidor B, et al. Among authors: baron s. Am J Med Genet A. 2009 Feb 15;149A(4):788-92. doi: 10.1002/ajmg.a.32343. Am J Med Genet A. 2009. PMID: 18478593 No abstract available.

5

Familial frameshift SRY mutation inherited from a mosaic father with testicular dysgenesis syndrome.

Isidor B, Capito C, Paris F, Baron S, Corradini N, Cabaret B, Leclair MD, Giraud M, Martin-Coignard D, David A, Sultan C, Le Caignec C. Isidor B, et al. Among authors: baron s. J Clin Endocrinol Metab. 2009 Sep;94(9):3467-71. doi: 10.1210/jc.2009-0226. Epub 2009 Jun 16. J Clin Endocrinol Metab. 2009. PMID: 19531589

6

Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxia.

Isidor B, Pichon O, Baron S, David A, Le Caignec C. Isidor B, et al. Among authors: baron s. Am J Med Genet A. 2010 Jan;152A(1):175-80. doi: 10.1002/ajmg.a.33152. Am J Med Genet A. 2010. PMID: 20014135

7

Axial spondylometaphyseal dysplasia: Confirmation and further delineation of a new SMD with retinal dystrophy.

Isidor B, Baron S, Khau van Kien P, Bertrand AM, David A, Le Merrer M. Isidor B, et al. Among authors: baron s. Am J Med Genet A. 2010 Jun;152A(6):1550-4. doi: 10.1002/ajmg.a.33397. Am J Med Genet A. 2010. PMID: 20503334

8

Constitutional telomeric association (Y;7) in a patient with a female phenotype.

Beneteau C, Baron S, David A, Jossic F, Poulain D, Schmitt S, Leclair MD, Piloquet P, Le Caignec C. Beneteau C, et al. Among authors: baron s. Am J Med Genet A. 2013 Jun;161A(6):1436-41. doi: 10.1002/ajmg.a.35889. Epub 2013 Apr 23. Am J Med Genet A. 2013. PMID: 23613342 Review.

9

Growth patterns of patients with Noonan syndrome: correlation with age and genotype.

Cessans C, Ehlinger V, Arnaud C, Yart A, Capri Y, Barat P, Cammas B, Lacombe D, Coutant R, David A, Baron S, Weill J, Leheup B, Nicolino M, Salles JP, Verloes A, Tauber M, Cavé H, Edouard T. Cessans C, et al. Among authors: baron s. Eur J Endocrinol. 2016 May;174(5):641-50. doi: 10.1530/EJE-15-0922. Epub 2016 Feb 22. Eur J Endocrinol. 2016. PMID: 26903553

10

Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys.

Martinerie L, Morel Y, Gay CL, Pienkowski C, de Kerdanet M, Cabrol S, Lecointre C, Coutant R, Baron S, Colle M, Brauner R, Thibaud E, Leger J, Nihoul-Fekete C, Bouvattier C. Martinerie L, et al. Among authors: baron s. Eur J Endocrinol. 2012 Apr;166(4):687-94. doi: 10.1530/EJE-11-0756. Epub 2012 Jan 11. Eur J Endocrinol. 2012. PMID: 22236473

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

1,252 results

Search Page

Filters