Publications by authors named "Ozden Sanal"

89Publications

B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancy.

Scand J Immunol 2018 Oct;88(4):e12709

Department of Pediatrics, Division of Pediatric Immunology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1111/sji.12709
Publisher Site
http://dx.doi.org/10.1111/sji.12709DOI Listing
October 2018

Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome.

Bone Marrow Transplant 2018 03 21;53(3):339-343. Epub 2017 Dec 21.

Faculty of Medicine, Department of Pediatrics, Division of Bone Marrow Transplantation Unit, Hacettepe University, Sıhhiye, 06100, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41409-017-0040-1DOI Listing
March 2018

A novel mutation in TAP1 gene leading to MHC class I deficiency: Report of two cases and review of the literature.

Clin Immunol 2017 05 2;178:74-78. Epub 2017 Feb 2.

Department of Pediatrics, Division of Immunology, Hacettepe University Faculty of Medicine, 06100 Sıhhiye, Ankara, Turkey. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clim.2017.01.011DOI Listing
May 2017

Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.

Turk J Pediatr 2017 ;59(5):555-560

Division of Pediatric Immunology, Hacettepe University Faculty of Medicine, Ankara.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.24953/turkjped.2017.05.008DOI Listing
January 2019

Low T Cell Numbers Resembling T-B+ SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations.

J Clin Immunol 2017 01 30;37(1):18-21. Epub 2016 Nov 30.

Department of Pediatric Immunology, Hacettepe University of Medicine, İhsan Doğramacı Children's Hospital, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10875-016-0356-4DOI Listing
January 2017

Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients.

Turk J Pediatr 2016 ;58(4):356-361

Division of Immunology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.24953/turkjped.2016.04.002DOI Listing
July 2017

Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS.

Turk J Pediatr 2015 Mar-Apr;57(2):141-5

Division of Immunology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara.

View Article

Download full-text PDF

Source
August 2016

CVID Associated with Systemic Amyloidosis.

Case Reports Immunol 2015 4;2015:879179. Epub 2015 Aug 4.

Division of Immunology, Department of Pediatrics, Hacettepe University Faculty of Medicine, 06100 Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2015/879179DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540992PMC
September 2015

STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation.

Clin Immunol 2015 Dec 25;161(2):316-23. Epub 2015 Jun 25.

Hacettepe University, Institute of Child Health, Department of Pediatric Immunology, Sihhiye, 06100 Ankara, Turkey. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clim.2015.06.010DOI Listing
December 2015

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R.

Haematologica 2015 Jun 13;100(6):e216-9. Epub 2015 Mar 13.

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Austria

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3324/haematol.2014.120980DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450632PMC
June 2015

Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion.

Pediatr Allergy Immunol 2014 Dec 31;25(8):817-9. Epub 2014 Oct 31.

Division of Pediatric Allergy and Immunology, Cukurova University, Adana, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/pai.12285DOI Listing
December 2014

A novel mutation in leukocyte adhesion deficiency type II/CDGIIc.

J Clin Immunol 2014 Nov 21;34(8):1009-14. Epub 2014 Sep 21.

Section of Pediatric Immunology, Hacettepe University, İhsan Doğramacı Children's Hospital , Ankara, Turkey,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10875-014-0091-7DOI Listing
November 2014

Progressive neurodegenerative syndrome in a patient with X-linked agammaglobulinemia receiving intravenous immunoglobulin therapy.

Cogn Behav Neurol 2014 Sep;27(3):155-9

*Institute of Neurological Sciences and Psychiatry †Department of Neurology, Hacettepe University, Ankara, Turkey ‡Department of Pediatrics, Immunology-Allergy, Akdeniz University, Faculty of Medicine, Antalya, Turkey §Department of Immunology, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/WNN.0000000000000037DOI Listing
September 2014

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia.

Blood 2014 Jul;124(4):655-7

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, AustriaDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood-2014-03-564930DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110665PMC
July 2014

Kindlin-3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III.

J Allergy Clin Immunol 2014 Apr 15;133(4):1215-8. Epub 2013 Dec 15.

Emma Children's Hospital, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jaci.2013.10.020DOI Listing
April 2014

Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL.

Mol Immunol 2013 Dec 1;56(4):354-7. Epub 2013 Aug 1.

Department of Pediatrics, Hacettepe University Ihsan Doğramacı Childrens Hospital, Ankara, Turkey. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.molimm.2013.05.004DOI Listing
December 2013

Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients.

J Allergy Clin Immunol 2013 Nov 31;132(5):1156-1163.e5. Epub 2013 Jul 31.

Immunology Department and GenKök Laboratory of Immunology, Faculty of Medicine, University of Erciyes, Kayseri, Turkey. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jaci.2013.05.039DOI Listing
November 2013

A novel mutation in the complement component 3 gene in a patient with selective IgA deficiency.

J Clin Immunol 2013 Jan 21;33(1):127-33. Epub 2012 Sep 21.

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, AKH BT 25.3, A-1090, Vienna, Austria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10875-012-9775-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555245PMC
January 2013

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients.

Eur J Pediatr 2012 Oct 19;171(10):1527-31. Epub 2012 Jun 19.

Division of Pediatric Immunology, Department of Pediatrics, Hacettepe University Faculty of Medicine, 06100 Ankara, Turkey.

View Article

Download full-text PDF

Source
http://link.springer.com/content/pdf/10.1007/s00431-012-1765
Web Search
http://link.springer.com/10.1007/s00431-012-1765-x
Publisher Site
http://dx.doi.org/10.1007/s00431-012-1765-xDOI Listing
October 2012

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma.

Clin Rheumatol 2012 Jul 11;31(7):1123-6. Epub 2012 May 11.

Department of Pediatric Nephrology and Rheumatology, Faculty of Medicine, Hacettepe University, Ankara 06100, Turkey.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s10067-012-1978-4
Publisher Site
http://dx.doi.org/10.1007/s10067-012-1978-4DOI Listing
July 2012

Thirty years of primary immunodeficiencies in Turkey.

Ann N Y Acad Sci 2011 Nov;1238:15-23

Immunology Division, Hacettepe University Children's Hospital, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1749-6632.2011.06242.xDOI Listing
November 2011

Association of tumour necrosis factor-alpha -308 G/A polymorphism with primary open-angle glaucoma.

Clin Exp Ophthalmol 2012 May-Jun;40(4):e156-62. Epub 2011 Jul 26.

Department of Ophthalmology, Selcuk University, Meram Medical Faculty, Konya, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1442-9071.2011.02595.xDOI Listing
August 2012

Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation.

Pediatr Transplant 2012 Aug 27;16(5):E167-71. Epub 2011 Apr 27.

Department of Pediatrics, Section of Pediatric Immunology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1399-3046.2011.01491.xDOI Listing
August 2012

Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.

Turk J Pediatr 2010 Nov-Dec;52(6):576-81

Division of Immunology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
April 2011

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries.

Authors:
Ludovic de Beaucoudrey Arina Samarina Jacinta Bustamante Aurélie Cobat Stéphanie Boisson-Dupuis Jacqueline Feinberg Saleh Al-Muhsen Lucile Jannière Yoann Rose Maylis de Suremain Xiao-Fei Kong Orchidée Filipe-Santos Ariane Chapgier Capucine Picard Alain Fischer Figen Dogu Aydan Ikinciogullari Gonul Tanir Sami Al-Hajjar Suliman Al-Jumaah Husn H Frayha Zobaida AlSum Sulaiman Al-Ajaji Abdullah Alangari Abdulaziz Al-Ghonaium Parisa Adimi Davood Mansouri Imen Ben-Mustapha Judith Yancoski Ben-Zion Garty Carlos Rodriguez-Gallego Isabel Caragol Necil Kutukculer Dinakantha S Kumararatne Smita Patel Rainer Doffinger Andrew Exley Olle Jeppsson Janine Reichenbach David Nadal Yaryna Boyko Barbara Pietrucha Suzanne Anderson Michael Levin Liliane Schandené Kinda Schepers André Efira Françoise Mascart Masao Matsuoka Tatsunori Sakai Claire-Anne Siegrist Klara Frecerova Renate Blüetters-Sawatzki Jutta Bernhöft Joachim Freihorst Ulrich Baumann Darko Richter Filomeen Haerynck Frans De Baets Vas Novelli David Lammas Christiane Vermylen David Tuerlinckx Chris Nieuwhof Malgorzata Pac Walther H Haas Ingrid Müller-Fleckenstein Bernhard Fleckenstein Jacob Levy Revathi Raj Aileen Cleary Cohen David B Lewis Steven M Holland Kuender D Yang Xiaochuan Wang Xiaohong Wang Liping Jiang Xiqiang Yang Chaomin Zhu Yuanyuan Xie Pamela Pui Wah Lee Koon Wing Chan Tong-Xin Chen Gabriela Castro Ivelisse Natera Ana Codoceo Alejandra King Liliana Bezrodnik Daniela Di Giovani Maria Isabel Gaillard Dewton de Moraes-Vasconcelos Anete Sevciovic Grumach Alberto Jose da Silva Duarte Ruth Aldana Francisco Javier Espinosa-Rosales Mohammed Bejaoui Ahmed Aziz Bousfiha Jamila El Baghdadi Namik Ozbek Guzide Aksu Melike Keser Ayper Somer Nevin Hatipoglu Cigdem Aydogmus Suna Asilsoy Yildiz Camcioglu Saniye Gülle Tuba T Ozgur Meteran Ozen Matias Oleastro Andrea Bernasconi Setareh Mamishi Nima Parvaneh Sergio Rosenzweig Ridha Barbouche Sigifredo Pedraza Yu Lung Lau Mohammad S Ehlayel Claire Fieschi Laurent Abel Ozden Sanal Jean-Laurent Casanova

Medicine (Baltimore) 2010 Nov;89(6):381-402

Laboratory of Human Genetics of Infectious Diseases U980, Institut National de la Santé et de la Recherche Médicale, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MD.0b013e3181fdd832DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129625PMC
November 2010

Hereditary C1q deficiency: a new family with C1qA deficiency.

Turk J Pediatr 2010 Mar-Apr;52(2):184-6

Division of Immunology, Department of Pediatrics, Hacettepe University, Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
August 2010

Multifocal leiomyosarcomatosis in a 6-year-old child with epidermodysplasia verruciformis and immune defect.

J Pediatr Surg 2009 Jul;44(7):e5-8

Department of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara 06100, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jpedsurg.2009.04.011DOI Listing
July 2009

Interleukin-12/-23 receptor beta 1 deficiency in an infant with draining BCG lymphadenitis.

Pediatr Int 2009 Apr;51(2):310-2

Department of Pediatrics, Dr Behçet Uz Children's Research and Training Hospital, Izmir, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1442-200X.2009.02818.xDOI Listing
April 2009

Parvovirus B19-induced persistent pure red cell aplasia in a child with T-cell immunodeficiency.

Pediatr Hematol Oncol 2009 Mar;26(2):63-8

Hacettepe University, Pediatric Hematology Unit, 06100-Sihhiye, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/08880010902754735DOI Listing
March 2009

LAD-1/variant syndrome is caused by mutations in FERMT3.

Blood 2009 May 8;113(19):4740-6. Epub 2008 Dec 8.

Department of Blood Cell Research, Sanquin Research and Landsteiner Laboratory, Academic Medical Center, University of Amsterdam, Emma Children's Hospital, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood-2008-10-182154DOI Listing
May 2009

Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency.

Eur J Pediatr 2009 Jan 29;168(1):87-93. Epub 2008 May 29.

Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Dr. Molewaterplein 50, 3015 GE, Rotterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00431-008-0718-xDOI Listing
January 2009

Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up.

Clin Rheumatol 2008 Oct 28;27(10):1317-20. Epub 2008 May 28.

Pediatric Nephrology and Rheumatology Unit, Faculty of Medicine, Hacettepe University, 06100, Sihhiye, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10067-008-0911-3DOI Listing
October 2008

Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.

J Pediatr Hematol Oncol 2007 May;29(5):327-9

Division of Immunology, Hacettepe University Children's Hospital, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MPH.0b013e318059c236DOI Listing
May 2007

A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis.

Pediatr Infect Dis J 2007 Apr;26(4):366-8

Divisions of Immunology, Hacettepe University Children's Hospital, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/01.inf.0000258696.64507.0fDOI Listing
April 2007

A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.

Turk J Pediatr 2006 Oct-Dec;48(4):362-4

Immunology Unit, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
April 2007

Natural history and early diagnosis of LAD-1/variant syndrome.

Blood 2007 Apr 21;109(8):3529-37. Epub 2006 Dec 21.

Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.

View Article

Download full-text PDF

Source
http://www.bloodjournal.org/content/109/8/3529.full.pdf
Web Search
http://www.bloodjournal.org/cgi/doi/10.1182/blood-2006-05-02
Publisher Site
http://dx.doi.org/10.1182/blood-2006-05-021402DOI Listing
April 2007

Recurrent Salmonella bacteremia in interleukin-12 receptor beta1 deficiency.

J Trop Pediatr 2006 Aug 10;52(4):296-8. Epub 2006 Mar 10.

Inonu University, Faculty of Medicine, Division of Pediatric Infectious Disease, Malatya, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/tropej/fml001DOI Listing
August 2006

The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID).

Turk J Pediatr 2005 Jul-Sep;47(3):239-46

Division of Immunology, Department of Pediatrics Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
November 2005

Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia.

Turk J Pediatr 2004 Jul-Sep;46(3):208-13

Department of Molecular Biology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
November 2004

Antioxidant enzymes in red blood cells and lymphocytes of ataxia-telangiectasia patients.

Turk J Pediatr 2004 Jul-Sep;46(3):204-7

Department of Biochemistry, Hacettepe University Faculty of Medicine, Ankara, Turkey.

View Article

Download full-text PDF

Source
November 2004

Interleukin (IL)-12 and IL-23 are key cytokines for immunity against Salmonella in humans.

J Infect Dis 2004 Nov 7;190(10):1755-7. Epub 2004 Oct 7.

Medical Research Council Centre for Immune Regulation, Division of Immunity and Infection, University of Birmingham, Birmingham, Alabama, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1086/425021DOI Listing
November 2004

Malignant solid tumors associated with congenital immunodeficiency disorders.

Pediatr Hematol Oncol 2004 Jul-Aug;21(5):441-51

Department of Pediatric Oncology, Hacettepe University, Institute of Oncology, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/08880010490457231DOI Listing
January 2005

Antibody response to a seven-valent pneumococcal conjugated vaccine in patients with ataxia-telangiectasia.

J Clin Immunol 2004 Jul;24(4):411-7

Immunology Division, Ihsan Dogramaci Children's Hospital, Hacettepe University, 06100 Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1023/B:JOCI.0000029109.15355.baDOI Listing
July 2004

IL-12 receptor deficiency revisited: IL-23-mediated signaling is also impaired in human genetic IL-12 receptor beta1 deficiency.

Eur J Immunol 2003 Dec;33(12):3393-7

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/eji.200324343DOI Listing
December 2003

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).

J Clin Invest 2003 Aug;112(3):450-6

Unité de Recherhe sur le Développement Normal et Pathologique du Systéme Immunitaire, Hôpital Necker-Enfants Malades, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1172/JCI18264DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC166299PMC
August 2003

TCR dynamics in human mature T lymphocytes lacking CD3 gamma.

J Immunol 2003 Jun;170(12):5947-55

Inmunología, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4049/jimmunol.170.12.5947DOI Listing
June 2003

The relationship between periodontal status and peripheral levels of neutrophils in two consanguineous siblings with severe congenital neutropenia: case reports.

Quintessence Int 2003 Mar;34(3):221-6

Department of Periodontology, Faculty of Dentistry, Hacettepe University, Ankara, Turkey.

View Article

Download full-text PDF

Source
March 2003

Comprehensive scanning of the ATM gene with DOVAM-S.

Hum Mutat 2003 Feb;21(2):123-31

Department of Molecular Genetics, City of Hope National Medical Center, Duarte, California 91010-3000, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.10158DOI Listing
February 2003

Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome.

Turk J Pediatr 2002 Oct-Dec;44(4):357-9

Department of Pediatrics, Uludag University Faculty of Medicine, Bursa, Turkey.

View Article

Download full-text PDF

Source
February 2003

Genetics, cytokines and human infectious disease: lessons from weakly pathogenic mycobacteria and salmonellae.

Nat Genet 2002 Sep;32(1):97-105

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://www.nature.com/articles/ng0902-97
Publisher Site
http://dx.doi.org/10.1038/ng0902-97DOI Listing
September 2002

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

J Clin Immunol 2002 Jul;22(4):237-43

Hacettepe University, Ihsan Doğramaci Children's Hospital, Immunology Division, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1023/a:1016045026204DOI Listing
July 2002

Early diagnosis of ataxia-telangiectasia using radiosensitivity testing.

J Pediatr 2002 Jun;140(6):724-31

Department of Pathology, UCLA School of Medicine, Los Angeles, California 90095-1732, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1067/mpd.2002.123879DOI Listing
June 2002

Hodgkin's disease and ataxia telangiectasia with pulmonary cavities.

Pediatr Pulmonol 2002 May;33(5):399-403

Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, Ankara, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ppul.10057DOI Listing
May 2002

Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.

Am J Med Genet 2002 Apr;108(4):333-6

Department of Pediatrics, Faculty of Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.10296DOI Listing
April 2002

Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations.

Exp Hematol 2002 Mar;30(3):252-61

Central Laboratory Netherlands Blood Transfusion Service (CLB) and Laboratory for Experimental and Clinical Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0301-472x(01)00782-2DOI Listing
March 2002