Your search returned 67 results.

Results
	1.	[Beta-thalassemia major: what is the situation in France?]. [electronic resource] by Badens, Catherine Thuret, Isabelle Producer: 20091223 In: La Revue du praticien vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	2.	Human Mendelian diseases related to abnormalities of the RNA exosome or its cofactors. [electronic resource] by Fabre, Alexandre Badens, Catherine Producer: 20141024 In: Intractable & rare diseases research vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Advances in understanding the pathogenesis of the red cell volume disorders. [electronic resource] by Badens, Catherine Guizouarn, Hélène Producer: 20170606 In: British journal of haematology vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A novel mutation (delAACT) in the tyrosinase gene in a Cameroonian black with type 1A oculocutaneous albinism. [electronic resource] by Badens, Catherine Courrier, Sébastien Aquaron, Robert Producer: 20060622 In: Journal of dermatological science vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects]. [electronic resource] by Joly, Philippe Pondarre, Corinne Badens, Catherine Producer: 20150826 In: Annales de biologie clinique vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Syndromic diarrhea/Tricho-hepato-enteric syndrome. [electronic resource] by Fabre, Alexandre Martinez-Vinson, Christine Goulet, Olivier Badens, Catherine Producer: 20130723 In: Orphanet journal of rare diseases vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient. [electronic resource] by Agouti, Imane Bennani, Mohcine Levy, Nicolas Giordano, Piero Badens, Catherine Producer: 20090618 In: Hemoglobin vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Beta-thalassemia intermedia due to two novel mutations in the promoter region of the beta-globin gene. [electronic resource] by Agouti, Imane Bennani, Mohcine Nezri, Meyer Levy, Nicolas Badens, Catherine Producer: 20080324 In: European journal of haematology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Compound heterozygosity for unstable hemoglobin Genova and beta(o)-thalassemia associated with early onset of thalassemia major syndrome. [electronic resource] by Badens, Catherine Paolasso, Chantal Fossat, Chantal Wajcman, Henri Thuret, Isabelle Producer: 20060801 In: Haematologica vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	10.	Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity. [electronic resource] by Agouti, Imane Badens, Catherine Abouyoub, Ahmed Levy, Nicolas Bennani, Mohcine Producer: 20090303 In: Genetic testing vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Senicapoc: a potent candidate for the treatment of a subset of hereditary xerocytosis caused by mutations in the Gardos channel. [electronic resource] by Rapetti-Mauss, Raphael Soriani, Olivier Vinti, Henri Badens, Catherine Guizouarn, Hélène Producer: 20180212 In: Haematologica vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island. [electronic resource] by Muszlak, Mathias Pissard, Serge Badens, Catherine Chamouine, Abdourahim Maillard, Olivier Thuret, Isabelle Producer: 20160324 In: Hemoglobin vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder. [electronic resource] by Fabre, Alexandre André, Nicolas Breton, Anne Broué, Pierre Badens, Catherine Roquelaure, Bertrand Producer: 20070508 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Thalassemia intermedia due to a novel mutation in the second intervening sequence of the beta-globin gene. [electronic resource] by Agouti, Imane Bennani, Mohcine Ahmed, Abouyoub Barakat, Amina Mohamed, Khattab Badens, Catherine Producer: 20080109 In: Hemoglobin vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Severe atazanavir-associated hyperbilirubinemia revealing Canton G6PD deficiency in an Asian HIV-infected patient. [electronic resource] by Javelle, Emilie Oliver, Manuela Savini, Hélène Aubry, Camille Badens, Catherine Simon, Fabrice Producer: 20120325 In: AIDS (London, England) vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A new ATRX mutation in a patient with acquired α-thalassemia myelodysplastic syndrome. [electronic resource] by Herbaux, Charles Badens, Catherine Guidez, Stéphanie Lacoste, Caroline Maboudou, Patrice Rose, Christian Producer: 20130430 In: Hemoglobin vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Comparative evaluation of the depletion-red cell exchange program with the Spectra Optia and the isovolemic hemodilution-red cell exchange method with the COBE Spectra in sickle cell disease patients. [electronic resource] by Poullin, Pascale Sanderson, Frederick Bernit, Emmanuelle Brun, Marion Berdah, Yael Badens, Catherine Producer: 20170403 In: Journal of clinical apheresis vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Four globin gene defects in a healthy child. [electronic resource] by Badens, Catherine Merono, Francoise Martini, Nathalie Lena-Russo, Danielle Gulbis, Beatrice Thuret, Isabelle Producer: 20030711 In: Haematologica vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	19.	Management of syndromic diarrhea/tricho-hepato-enteric syndrome: A review of the literature. [electronic resource] by Fabre, Alexandre Bourgeois, Patrice Coste, Marie-Edith Roman, Céline Barlogis, Vincent Badens, Catherine Publication details: Intractable & rare diseases research Aug 2017 In: Intractable & rare diseases research vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Analytical evaluation of the Tosoh HLC-723 G8 automated HPLC analyzer for hemoglobin analysis in beta-thalassemia mode. [electronic resource] by Merono, Françoise Agouti, Imane Bonello-Palot, Nathalie Paolasso, Chantal Levy, Nicolas Badens, Catherine Producer: 20110701 In: Clinical biochemistry vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

1
2
3
4
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 67 results.