Kamran Moradkhani

Kamran Moradkhani

UNVERIFIED PROFILE

Are you Kamran Moradkhani?   Register this Author

Register author
Kamran Moradkhani

Kamran Moradkhani

Publications by authors named "Kamran Moradkhani"

Are you Kamran Moradkhani?   Register this Author

26Publications

397Reads

11Profile Views

Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.

Prenat Diagn 2019 Sep 5;39(10):871-882. Epub 2019 Jul 5.

Fédération de Génétique, Centre Hospitalier Intercommunal Poissy-St-Germain-en-Laye, Poissy, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pd.5498DOI Listing
September 2019

Morphokinetic parameters in chromosomal translocation carriers undergoing preimplantation genetic testing.

Reprod Biomed Online 2019 Feb 7;38(2):177-183. Epub 2018 Dec 7.

Service de Médecine de la Reproduction, CHU Nantes, 38 boulevard Jean Monnet, Nantes Cedex 44093, France; Centre de Recherche en Transplantation et Immunologie UMR 1064, INSERM, Université de Nantes, Nantes, France; Faculté de médecine, Université de Nantes, Nantes, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.rbmo.2018.11.006DOI Listing
February 2019

Pitfalls in the biological diagnosis of common hemoglobin disorders.

Ann Biol Clin (Paris) 2015 Sep-Oct;73(5):535-43

Service de génétique médicale, CHU de Nantes, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/abc.2015.1074DOI Listing
August 2016

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.

Nucleic Acids Res 2014 Jan 16;42(Database issue):D1063-9. Epub 2013 Oct 16.

The Pennsylvania State University, Center for Comparative Genomics and Bioinformatics, University Park, PA, USA, Department of Applied Biomedical Science, Faculty of Health Sciences, University of Malta, Msida, Malta, MGC-Department of Cell Biology and Genetics, Erasmus MC, Faculty of Medicine and Health Sciences, Rotterdam, The Netherlands, Department of Computer Engineering and Informatics, University of Patras, Faculty of Engineering, Patras, Greece, Department of Pharmacy, University of Patras, School of Health Sciences, Patras, Greece, Department of Medical Genetics, Laboratory of Cytogenetics, Institute of Biology, Nantes, France, Hôpital Edouard Herriot, Unité de Pathologie Moléculaire du Globule Rouge, Lyon, France, Department of Computer and Informatics Engineering, Technological Educational Institute of Western Greece, Patras, Greece, INSERM U955, CHU Henri Mondor, Creteil, France and Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, USA.

View Article

Download full-text PDF

Source
http://nar.oxfordjournals.org/content/early/2013/10/16/nar.g
Web Search
http://nar.oxfordjournals.org/lookup/doi/10.1093/nar/gkt911
Publisher Site
http://dx.doi.org/10.1093/nar/gkt911DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964999PMC
January 2014

Pitfalls in the genetic diagnosis of Hb S.

Clin Biochem 2013 Mar 17;46(4-5):291-9. Epub 2012 Sep 17.

AP-HP, Hôpital H. Mondor-A. Chenevier, Service de Biochimie et Génétique, Créteil, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clinbiochem.2012.08.018DOI Listing
March 2013

Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia.

Blood Cells Mol Dis 2013 Feb 7;50(2):110-4. Epub 2012 Sep 7.

Laboratoire d'hématologie moléculaire et cellulaire, Institut Pasteur de Tunis, 13 place Pasteur, Tunis-Le-Belvédère, Tunisia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bcmd.2012.08.005DOI Listing
February 2013

Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis.

Blood 2012 Oct 23;120(15):3136-41. Epub 2012 Aug 23.

Service de Médecine Interne, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris (AP-HP), Université Paris Est, Créteil, France.

View Article

Download full-text PDF

Source
http://www.bloodjournal.org/cgi/doi/10.1182/blood-2012-04-42
Publisher Site
http://dx.doi.org/10.1182/blood-2012-04-424184DOI Listing
October 2012

Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutations.

Blood Cells Mol Dis 2012 Mar 30;48(3):154-65. Epub 2012 Jan 30.

Laboratory of Clinical Molecular Diagnostics, Institute of Biochemistry and Clinical Biochemistry, Catholic University of Rome, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bcmd.2012.01.001DOI Listing
March 2012

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi Arabia.

BMC Res Notes 2011 Oct 24;4:436. Epub 2011 Oct 24.

Hematology Research Lab, King Fahd Medical Research Centre, Faculty of Medicine, King Abdulaziz University, P,O, Box 80215, Jeddah 21589, Kingdom of Saudi Arabia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1756-0500-4-436DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3208249PMC
October 2011

Abnormal haemoglobins: detection & characterization.

Indian J Med Res 2011 Oct;134:538-46

INSERM, Université Paris-Est, Faculté de Médecine, Créteil, France.

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237254PMC
October 2011