References analysis of the Wikipedia article "ВХИМ синдром" in the Serbian version

doi.org

Compagno, Nicolã²; Malipiero, Giacomo; Cinetto, Francesco; Agostini, Carlo (2014). „Immunoglobulin Replacement Therapy in Secondary Hypogammaglobulinemia”. Frontiers in Immunology. 5: 626. PMC 4259107 

. PMID 25538710. doi:10.3389/fimmu.2014.00626 

ZUELZER WW (1964). „"Myelokathexis"--A New Form of Chronic Granulocytopenia. Report of a Case”. New England Journal of Medicine. 270: 699—704. PMID 14101065. doi:10.1056/NEJM196404022701402.

Gorlin, R. J.; Gelb, B.; Diaz, G. A.; Lofsness, K. G.; Pittelkow, M. R.; Fenyk Jr, J. R. (2000). „WHIM syndrome, an autosomal dominant disorder: Clinical, hematological, and molecular studies”. The American Journal of Medical Genetics. 91 (5): 368—376. PMID 10767001. doi:10.1002/(SICI)1096-8628(20000424)91:5<368::AID-AJMG10>3.0.CO;2-9.

Kawai, Toshinao; Malech, Harry L. (5. 1. 2009). „WHIM Syndrome: Congenital Immune Deficiency Disease”. Current Opinion in Hematology. 16 (1): 20—26. ISSN 1065-6251. PMC 2673024 

. PMID 19057201. doi:10.1097/MOH.0b013e32831ac557.

. Wetzler M, Talpaz M, Kleinerman ES, King A, Huh YO, Gutterman JU, Kurzrock R (1990). „A new familial immunodeficiency disorder characterized by severe neutropenia, a defective marrow release mechanism, and hypogammaglobulinemia”. The American Journal of Medicine. 89 (5): 663—672. PMID 2239986. doi:10.1016/0002-9343(90)90187-I.

ZUELZER WW (1964). „"Myelokathexis"--a New Form of Chronic Granulocytopenia. Report of a Case”. New England Journal of Medicine. 270: 699—704. PMID 14101065. doi:10.1056/NEJM196404022701402.. [PubMed] [Google Scholar]

Roland J, Murphy BJ, Ahr B, Robert-Hebmann V, Delauzun V, Nye KE, Devaux C, Biard-Piechaczyk M (2003). „Role of the intracellular domains of CXCR4 in SDF-1-mediated signaling”. Blood. 101 (2): 399—406. PMID 12393663. doi:10.1182/blood-2002-03-0978.

Bassan, R.; Viero, P.; Minetti, B.; Comotti, B.; Barbui, T. (1984). „Myelokathexis: A rare form of chronic benign granulocytopenia”. British Journal of Haematology. 58 (1): 115—117. PMID 6466565. doi:10.1111/j.1365-2141.1984.tb06065.x.

O'Regan, S.; Newman, A. J.; Graham, R. C. (1977). „Neutropenia with marrow hyperplasia”. Am J Dis Child. 131 (6): 655—658. PMID 868817. doi:10.1001/archpedi.1977.02120190049011.

Frodl, Reinhard; Gierschik, Peter; Moepps, Barbara (1998). „Genomic Organization and Expression of the CXCR4 Gene in Mouse and Man: Absence of a Splice Variant Corresponding to Mouse CXCR4-B in Human Tissues”. Journal of Receptors and Signal Transduction. 18 (4–6): 321—344. PMID 9879064. doi:10.3109/10799899809047750.

Kawai, Toshinao; Choi, Uimook; Cardwell, Lanise; Deravin, Suk See; Naumann, Nora; Whiting-Theobald, Narda L.; Linton, Gilda F.; Moon, Jaehyun; Murphy, Philip M.; Malech, Harry L. (2007). „WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus–truncated CXCR4”. Blood. 109 (1): 78—84. PMC 1785067 

. PMID 16946301. doi:10.1182/blood-2006-05-025296.

Hernandez, Paolo A.; Gorlin, Robert J.; Lukens, John N.; Taniuchi, Shoichiro; Bohinjec, Jože; Francois, Fleur; Klotman, Mary E.; Diaz, George A. (2003). „Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease”. Nature Genetics. 34 (1): 70—74. PMID 12692554. S2CID 25010857. doi:10.1038/ng1149.

Lagane, Bernard; Chow, Ken Y. C.; Balabanian, Karl; Levoye, Angélique; Harriague, Julie; Planchenault, Thierry; Baleux, Françoise; Gunera-Saad, Nathalie; Arenzana-Seisdedos, Fernando; Bachelerie, Françoise (2008). „CXCR4 dimerization and β-arrestin–mediated signaling account for the enhanced chemotaxis to CXCL12 in WHIM syndrome”. Blood. 112 (1): 34—44. PMID 18436740. S2CID 7067287. doi:10.1182/blood-2007-07-102103.

Balabanian, Karl; Levoye, Angélique; Klemm, Lysiane; Lagane, Bernard; Hermine, Olivier; Harriague, Julie; Baleux, Françoise; Arenzana-Seisdedos, Fernando; Bachelerie, Françoise (2008). „Leukocyte analysis from WHIM syndrome patients reveals a pivotal role for GRK3 in CXCR4 signaling”. Journal of Clinical Investigation. 118 (3): 1074—1084. PMC 2242619 

. PMID 18274673. doi:10.1172/JCI33187.

Wetzler, Meir; Talpaz, Moshe; Kleinerman, Eugenie S.; King, Alice; Huh, Yang O.; Gutterman, Jordan U.; Kurzrock, Razelle (1990). „A new familial immunodeficiency disorder characterized by severe neutropenia, a defective marrow release mechanism, and hypogammaglobulinemia”. The American Journal of Medicine. 89 (5): 663—672. PMID 2239986. doi:10.1016/0002-9343(90)90187-i.

McDermott, David H.; Lopez, Joseph; Deng, Francis; Liu, Qian; Ojode, Teresa; Chen, Haoqian; Ulrick, Jean; Kwatemaa, Nana; Kelly, Corin; Anaya-o'Brien, Sandra; Garofalo, Mary; Marquesen, Martha; Hilligoss, Dianne; Decastro, Rosamma; Malech, Harry L.; Murphy, Philip M. (2011). „AMD3100 is a potent antagonist at CXCR4R334X, a hyperfunctional mutant chemokine receptor and cause of WHIM syndrome”. Journal of Cellular and Molecular Medicine. 15 (10): 2071—2081. PMC 3071896 

. PMID 21070597. doi:10.1111/j.1582-4934.2010.01210.x.

McDermott, David H.; Liu, Qian; Ulrick, Jean; Kwatemaa, Nana; Anaya-o'Brien, Sandra; Penzak, Scott R.; Filho, Joao Oliveira; Priel, Debra A. Long; Kelly, Corin; Garofalo, Mary; Littel, Patricia; Marquesen, Martha M.; Hilligoss, Diane; Decastro, Rosamma; Fleisher, Thomas A.; Kuhns, Douglas B.; Malech, Harry L.; Murphy, Philip M. (2011). „The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome”. Blood. 118 (18): 4957—4962. PMC 3208300 

. PMID 21890643. doi:10.1182/blood-2011-07-368084.

Dale, David C.; Bolyard, Audrey Anna; Kelley, Merideth L.; Westrup, Ernest C.; Makaryan, Vahagn; Aprikyan, Andrew; Wood, Brent; Hsu, Frank J. (2011). „The CXCR4 antagonist plerixafor is a potential therapy for myelokathexis, WHIM syndrome”. Blood. 118 (18): 4963—4966. PMC 3673761 

. PMID 21835955. doi:10.1182/blood-2011-06-360586.

B-cell lymphoma in a patient with WHIM syndrome.Chae KM, Ertle JO (јануар 2001). „B-cell lymphoma in a patient with WHIM syndrome”. Tharp MD Journal of the American Academy of Dermatology. 44 (1): 124—8. PMID 11148489. doi:10.1067/mjd.2001.111337.

Imashuku S, Miyagawa A, Chiyonobu T, Ishida H, Yoshihara T, Teramura T, Kuriyama K, Imamura T, Hibi S, Morimoto A, Todo S Epstein-Barr virus-associated T-lymphoproliferative disease with hemophagocytic syndrome, followed by fatal intestinal B lymphoma in a young adult female with WHIM syndrome (август 2002). „Warts, hypogammaglobulinemia, infections, and myelokathexis”. Ann Hematol. 81 (8): 470—3. PMID 12224006. doi:10.1007/s00277-002-0489-9.

Kawai, Toshinao; Malech, Harry L. (2009). „Treatment and Prognosis У: WHIM Syndrome: Congenital Immune Deficiency Disease”. Current Opinion in Hematology. 16 (1): 20—26. ISSN 1065-6251. PMC 2673024 

. PMID 19057201. doi:10.1097/MOH.0b013e32831ac557.

nih.gov

ncbi.nlm.nih.gov

. PMID 25538710. doi:10.3389/fimmu.2014.00626 

Kawai, Toshinao; Malech, Harry L. (5. 1. 2009). „WHIM Syndrome: Congenital Immune Deficiency Disease”. Current Opinion in Hematology. 16 (1): 20—26. ISSN 1065-6251. PMC 2673024 

. PMID 19057201. doi:10.1097/MOH.0b013e32831ac557.

O'Regan, S.; Newman, A. J.; Graham, R. C. (1977). „Neutropenia with marrow hyperplasia”. Am J Dis Child. 131 (6): 655—658. PMID 868817. doi:10.1001/archpedi.1977.02120190049011.