Badens C - Search Results

1

Transfusion requirements and complication rate in β-thalassemia intermedia due to heterozygous β-globin gene mutation and triplicated α-globin genes.

Bonello-Palot N, Benoit A, Agouti I, Hamouda I, Brousse V; NaThalY Network; Badens C. Bonello-Palot N, et al. Among authors: badens c. Eur J Haematol. 2023 Nov;111(5):742-747. doi: 10.1111/ejh.14070. Epub 2023 Jul 30. Eur J Haematol. 2023. PMID: 37519097

2

[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille].

Lena-Russo D, Erny N, Serradimigni F, Badens C, Aubinaud M, Merono F, Paolasso C, Mattei JF, Giraud F. Lena-Russo D, et al. Among authors: badens c. Presse Med. 1996 Feb 3;25(4):151-3. Presse Med. 1996. PMID: 8728899 French.

3

Severe atazanavir-associated hyperbilirubinemia revealing Canton G6PD deficiency in an Asian HIV-infected patient.

Javelle E, Oliver M, Savini H, Aubry C, Badens C, Simon F. Javelle E, et al. Among authors: badens c. AIDS. 2012 Jan 14;26(2):249-51. doi: 10.1097/QAD.0b013e32834e1d33. AIDS. 2012. PMID: 22179231 No abstract available.

4

[Genetic abnormality of unrecognized hemoglobin: alpha-thalassemia].

Orsini A, Perrimond H, Lena D, Vovan L, Badens C. Orsini A, et al. Among authors: badens c. Arch Pediatr. 1996 Mar;3(3):210-2. doi: 10.1016/0929-693x(96)81168-7. Arch Pediatr. 1996. PMID: 8785556 French. No abstract available.

5

[Prevention of hemoglobinopathies in non-endemic countries].

Badens C. Badens C. Bull Soc Pathol Exot. 2001 May;94(2):98-100. Bull Soc Pathol Exot. 2001. PMID: 11475037 Review. French.

6

A novel mutation (delAACT) in the tyrosinase gene in a Cameroonian black with type 1A oculocutaneous albinism.

Badens C, Courrier S, Aquaron R. Badens C, et al. J Dermatol Sci. 2006 May;42(2):121-4. doi: 10.1016/j.jdermsci.2006.01.007. Epub 2006 Mar 6. J Dermatol Sci. 2006. PMID: 16517127 No abstract available.

7

Partial duplications of the ATRX gene cause the ATR-X syndrome.

Thienpont B, de Ravel T, Van Esch H, Van Schoubroeck D, Moerman P, Vermeesch JR, Fryns JP, Froyen G, Lacoste C, Badens C, Devriendt K. Thienpont B, et al. Among authors: badens c. Eur J Hum Genet. 2007 Oct;15(10):1094-7. doi: 10.1038/sj.ejhg.5201878. Epub 2007 Jun 20. Eur J Hum Genet. 2007. PMID: 17579672

8

Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder.

Fabre A, André N, Breton A, Broué P, Badens C, Roquelaure B. Fabre A, et al. Among authors: badens c. Am J Med Genet A. 2007 Mar 15;143A(6):584-8. doi: 10.1002/ajmg.a.31634. Am J Med Genet A. 2007. PMID: 17318842

9

[ATR-X syndrome: a new mutation in the XNP/ATRX gene near the helicase domain].

Giuliano F, Badens C, Richelme C, Levy N, Lambert JC. Giuliano F, et al. Among authors: badens c. Arch Pediatr. 2005 Sep;12(9):1372-5. doi: 10.1016/j.arcped.2005.03.053. Arch Pediatr. 2005. PMID: 16125058 French.

10

Hb Bruxelles, deletion of Phebeta42, shows a low oxygen affinity and low cooperativity of ligand binding.

Griffon N, Badens C, Lena-Russo D, Kister J, Bardakdjian J, Wajcman H, Marden MC, Poyart C. Griffon N, et al. Among authors: badens c. J Biol Chem. 1996 Oct 18;271(42):25916-20. doi: 10.1074/jbc.271.42.25916. J Biol Chem. 1996. PMID: 8824225 Free article.

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