Baumann C - Search Results

1

Brachytelephalangic chondrodysplasia punctata with severe spinal cord compression: report of four new cases.

Garnier A, Dauger S, Eurin D, Parisi I, Parenti G, Garel C, Delbecque K, Baumann C. Garnier A, et al. Among authors: baumann c. Eur J Pediatr. 2007 Apr;166(4):327-31. doi: 10.1007/s00431-006-0239-4. Epub 2006 Aug 26. Eur J Pediatr. 2007. PMID: 16937129

2

Abnormal abdominal situs: what and how should we look for?

Salomon LJ, Baumann C, Delezoide AL, Oury JF, Pariente D, Sebag G, Garel C. Salomon LJ, et al. Among authors: baumann c. Prenat Diagn. 2006 Mar;26(3):282-5. doi: 10.1002/pd.1401. Prenat Diagn. 2006. PMID: 16506280

3

Gracile bones, periostal appositions, hypomineralization of the cranial vault, and mental retardation in brothers: milder variant of osteocraniostenosis or new syndrome?

Verloes A, Garel C, Robertson S, Le Merrer M, Baumann C. Verloes A, et al. Among authors: baumann c. Am J Med Genet A. 2005 Aug 30;137(2):199-203. doi: 10.1002/ajmg.a.30360. Am J Med Genet A. 2005. PMID: 16086393

4

A new syndrome of congenital generalized osteosclerosis and bilateral polymicrogyria.

Titomanlio L, Baumann C, Bonyhay G, Huten Y, Oury JF, Vuillard E, Garel C, Terdjman P, Verloes A, Delezoide AL. Titomanlio L, et al. Among authors: baumann c. Am J Med Genet A. 2005 Sep 15;138(1):1-5. doi: 10.1002/ajmg.a.30914. Am J Med Genet A. 2005. PMID: 16097005

5

Severely delayed epiphyseal ossification dysplasia with normal stature.

Baumann C, Garel C, Vuillemain L, Hassan M, Verloes A. Baumann C, et al. Am J Med Genet A. 2003 Aug 1;120A(4):553-6. doi: 10.1002/ajmg.a.20046. Am J Med Genet A. 2003. PMID: 12884438

6

Humero-radial synostosis, microcephaly, short corpus callosum, and abnormal genitalia in sibs.

Guilherme R, Baumann C, Garel C, Huten Y, Oury JF, Delezoide AL. Guilherme R, et al. Among authors: baumann c. Am J Med Genet A. 2008 Jul 15;146A(14):1775-80. doi: 10.1002/ajmg.a.32380. Am J Med Genet A. 2008. PMID: 18553517 Review.

7

High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosis.

Guilmin-Crépon S, Garel C, Baumann C, Brémond-Gignac D, Bailleul-Forestier I, Magnier S, Castanet M, Czernichow P, VAN DEN Abbeele T, Léger J. Guilmin-Crépon S, et al. Among authors: baumann c. Pediatr Res. 2006 Oct;60(4):478-84. doi: 10.1203/01.pdr.0000238380.03683.cb. Epub 2006 Aug 28. Pediatr Res. 2006. PMID: 16940234

8

Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.

Spaggiari E, Baumann C, Alison M, Oury JF, Belarbi N, Dupont C, Guimiot F, Delezoide AL. Spaggiari E, et al. Among authors: baumann c. Eur J Med Genet. 2013 Jun;56(6):297-300. doi: 10.1016/j.ejmg.2013.03.003. Epub 2013 Mar 21. Eur J Med Genet. 2013. PMID: 23523603

9

Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome).

Sznajer Y, Baumann C, David A, Journel H, Lacombe D, Perel Y, Blouin P, Segura JF, Cezard JP, Peuchmaur M, Vulliamy T, Dokal I, Verloes A. Sznajer Y, et al. Among authors: baumann c. Eur J Pediatr. 2003 Dec;162(12):863-7. doi: 10.1007/s00431-003-1317-5. Epub 2003 Sep 30. Eur J Pediatr. 2003. PMID: 14648217 Review.

10

Neuropathic visceral dysmotility, brain cysts and calcifications, facial dysmorphism and developmental delay in two sibs. A new syndrome?

Hadchouel A, Bellaiche M, Baumann C, Darnaud G, El Ghoneimi A, Ferkdadji L, Elmaleh M, Verloes A. Hadchouel A, et al. Among authors: baumann c. Eur J Med Genet. 2005 Oct-Dec;48(4):367-76. doi: 10.1016/j.ejmg.2005.05.006. Epub 2005 Jun 16. Eur J Med Genet. 2005. PMID: 16378921

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