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Items: 1 to 50 of 148

1.

Proteome analysis of human neutrophil granulocytes from patients with monogenic disease using data-independent acquisition.

Grabowski P, Hesse S, Hollizeck S, Rohlfs M, Behrends U, Sherkat R, Tamary H, Ünal E, Somech R, Patıroğlu T, Canzar S, van der Werff Ten Bosch J, Klein C, Rappsilber J.

Mol Cell Proteomics. 2019 Jan 10. pii: mcp.RA118.001141. doi: 10.1074/mcp.RA118.001141. [Epub ahead of print]

2.

Endoscopic findings and esophageal cancer incidence among Fanconi Anemia patients participating in an endoscopic surveillance program.

Itskoviz D, Tamary H, Krasnov T, Yacobovich J, Sahar N, Zevit N, Shamir R, Ben-Bassat O, Leibovici Wiseman Y, Dickman R, Ringel Y, Dotan I, Goldberg Y, Morgenstern S, Levi Z.

Dig Liver Dis. 2019 Feb;51(2):242-246. doi: 10.1016/j.dld.2018.08.010. Epub 2018 Aug 18.

PMID:
30249500
3.

Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE).

Seo A, Gulsuner S, Pierce S, Ben-Harosh M, Shalev H, Walsh T, Krasnov T, Dgany O, Doulatov S, Tamary H, Shimamura A, King MC.

Hum Mol Genet. 2019 Jan 1;28(1):133-142. doi: 10.1093/hmg/ddy334.

PMID:
30247636
4.

Gray platelet syndrome mimicking atypical autoimmune lymphoproliferative syndrome: the key is in the blood smear.

Steinberg-Shemer O, Tamary H.

Blood. 2018 Jun 14;131(24):2737. doi: 10.1182/blood-2018-03-841940. No abstract available.

PMID:
29903870
5.

Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.

Shefer Averbuch N, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Yacobovich J, Kuperman AA, Kattamis A, Ben Barak A, Roth-Jelinek B, Chubar E, Shabad E, Dufort G, Ellis M, Wolach O, Pazgal I, Abu Quider A, Miskin H, Tamary H.

Eur J Haematol. 2018 Sep;101(3):297-304. doi: 10.1111/ejh.13097. Epub 2018 Jun 25.

PMID:
29786897
6.

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1.

Seo A, Steinberg-Shemer O, Unal S, Casadei S, Walsh T, Gumruk F, Shalev S, Shimamura A, Akarsu NA, Tamary H, King MC.

Proc Natl Acad Sci U S A. 2018 May 15;115(20):5241-5246. doi: 10.1073/pnas.1801796115. Epub 2018 Apr 30.

7.

Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia.

Wlodarski MW, Da Costa L, O'Donohue MF, Gastou M, Karboul N, Montel-Lehry N, Hainmann I, Danda D, Szvetnik A, Pastor V, Paolini N, di Summa FM, Tamary H, Quider AA, Aspesi A, Houtkooper RH, Leblanc T, Niemeyer CM, Gleizes PE, MacInnes AW.

Haematologica. 2018 Jun;103(6):949-958. doi: 10.3324/haematol.2017.177980. Epub 2018 Mar 29.

8.

A comparative prospective observational study of children and adults with immune thrombocytopenia: 2-year follow-up.

Schifferli A, Holbro A, Chitlur M, Coslovsky M, Imbach P, Donato H, Elalfy M, Graciela E, Grainger J, Holzhauer S, Riccheri C, Rodeghiero F, Ruggeri M, Tamary H, Uglova T, Wu R, Kühne T; Intercontinental Cooperative ITP Study Group (ICIS).

Am J Hematol. 2018 Jun;93(6):751-759. doi: 10.1002/ajh.25086. Epub 2018 Mar 30.

PMID:
29516627
9.

Labile plasma iron as an indicator of patient adherence to iron chelation treatment.

Steinberg-Shemer O, Yacobovich J, Cohen M, Cabantchik IZ, Tamary H.

Blood Cells Mol Dis. 2018 Jul;71:1-4. doi: 10.1016/j.bcmd.2018.01.001. Epub 2018 Jan 31.

PMID:
29395830
10.

Corrigendum to "X-linked elliptocytosis with impaired growth is related to mutated AMMECR1" [Gene 606C (2017) 47-52].

Basel-Vanagaite L, Pillar N, Isakov O, Smirin-Yosef P, Lagovsky I, Orenstein N, Salmon-Divon M, Tamary H, Zaft T, Bazak L, Meyerovitch J, Pelli T, Botchan S, Farberov L, Weissglas-Volkov D, Shomron N.

Gene. 2018 Feb 20;644:155. doi: 10.1016/j.gene.2017.11.051. Epub 2017 Nov 27. No abstract available.

PMID:
29174631
11.

Response of Symptomatic Persistent Chronic Disseminated Candidiasis to Corticosteroid Therapy in Immunosuppressed Pediatric Patients: Case Study and Review of the Literature.

Shkalim-Zemer V, Levi I, Fischer S, Tamary H, Yakobovich J, Avrahami G, Gilad G, Elitzur S, Yaniv I, Elhasid R, Manistersky M, Shalit I.

Pediatr Infect Dis J. 2018 Jul;37(7):686-690. doi: 10.1097/INF.0000000000001844.

PMID:
29140934
12.

Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.

Da Costa L, O'Donohue MF, van Dooijeweert B, Albrecht K, Unal S, Ramenghi U, Leblanc T, Dianzani I, Tamary H, Bartels M, Gleizes PE, Wlodarski M, MacInnes AW.

Eur J Med Genet. 2018 Nov;61(11):664-673. doi: 10.1016/j.ejmg.2017.10.017. Epub 2017 Oct 26. Review.

13.

Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.

Resnitzky P, Shaft D, Shalev H, Kapelushnik J, Dgany O, Krasnov T, Tamary H.

Eur J Haematol. 2017 Oct;99(4):366-371. doi: 10.1111/ejh.12931. Epub 2017 Aug 29.

PMID:
28755517
14.

Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.

Steinberg-Shemer O, Ulirsch JC, Noy-Lotan S, Krasnov T, Attias D, Dgany O, Laor R, Sankaran VG, Tamary H.

Cold Spring Harb Mol Case Stud. 2017 Nov 21;3(6). pii: a001941. doi: 10.1101/mcs.a001941. Print 2017 Nov.

15.

Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin.

Seo A, Ben-Harosh M, Sirin M, Stein J, Dgany O, Kaplelushnik J, Hoenig M, Pannicke U, Lorenz M, Schwarz K, Stockklausner C, Walsh T, Gulsuner S, Lee MK, Sendamarai A, Sanchez-Bonilla M, King MC, Cario H, Kulozik AE, Debatin KM, Schulz A, Tamary H, Shimamura A.

Blood. 2017 Aug 17;130(7):875-880. doi: 10.1182/blood-2017-02-768036. Epub 2017 May 30.

16.

Recommendations regarding splenectomy in hereditary hemolytic anemias.

Iolascon A, Andolfo I, Barcellini W, Corcione F, Garçon L, De Franceschi L, Pignata C, Graziadei G, Pospisilova D, Rees DC, de Montalembert M, Rivella S, Gambale A, Russo R, Ribeiro L, Vives-Corrons J, Martinez PA, Kattamis A, Gulbis B, Cappellini MD, Roberts I, Tamary H; Working Study Group on Red Cells and Iron of the EHA.

Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26.

17.

Molecular diagnosis of α-thalassemia in a multiethnic population.

Gilad O, Shemer OS, Dgany O, Krasnov T, Nevo M, Noy-Lotan S, Rabinowicz R, Amitai N, Ben-Dor S, Yaniv I, Yacobovich J, Tamary H.

Eur J Haematol. 2017 Jun;98(6):553-562. doi: 10.1111/ejh.12866. Epub 2017 Apr 6.

PMID:
28160324
18.

X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.

Basel-Vanagaite L, Pillar N, Isakov O, Smirin-Yosef P, Lagovsky I, Orenstein N, Salmon-Divon M, Tamary H, Zaft T, Bazak L, Meyerovitch J, Pelli T, Botchan S, Farberov L, Weissglas-Volkov D, Shomron N.

Gene. 2017 Mar 30;606:47-52. doi: 10.1016/j.gene.2017.01.001. Epub 2017 Jan 9. Erratum in: Gene. 2017 Nov 23;:.

PMID:
28089922
19.

Evaluating platelet function disorders in children with bleeding tendency - A single center study.

Tanous O, Steinberg Shemer O, Yacobovich J, Zoldan M, Horovitz Y, Yaniv I, Rabizadeh E, Tamary H, Nakav S, Lahav J.

Platelets. 2017 Nov;28(7):676-681. doi: 10.1080/09537104.2016.1257784. Epub 2017 Jan 6.

PMID:
28060550
20.

Quantitation of bleeding symptoms in a national registry of patients with inherited platelet disorders.

Revel-Vilk S, Richter C, Ben-Ami T, Yacobovich J, Aviner S, Ben-Barak A, Kuperman AA, Ben-Barak S, Kaplinsky C, Miskin H, Tamary H, Kenet G.

Blood Cells Mol Dis. 2017 Sep;67:59-62. doi: 10.1016/j.bcmd.2016.11.013. Epub 2016 Dec 18.

PMID:
27998672
21.

Anemia and markers of erythropoiesis in pediatric kidney transplant recipients compared to children with chronic renal failure.

Krause I, Davidovits M, Tamary H, Yutcis M, Dagan A.

Pediatr Transplant. 2016 Nov;20(7):958-962. doi: 10.1111/petr.12792. Epub 2016 Sep 12.

PMID:
27620552
22.

Distal limb anomalies in patients with congenital dyserythropoietic anemia.

Amir AZ, Horev G, Yacobovich J, Bennett M, Tamary H.

Am J Med Genet A. 2017 Feb;173(2):487-490. doi: 10.1002/ajmg.a.38012. Epub 2016 Oct 19.

PMID:
27759939
23.

Congenital Dyserythropoietic Anemia Type I.

Tamary H, Dgany O.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2009 Apr 21 [updated 2016 Aug 25].

24.

Inhaled corticosteroids increase blood neutrophil count by decreasing the expression of neutrophil adhesion molecules Mac-1 and L-selectin.

Pasternak Y, Yarden-Bilavsky H, Kodman Y, Zoldan M, Tamary H, Ashkenazi S.

Am J Emerg Med. 2016 Oct;34(10):1977-1981. doi: 10.1016/j.ajem.2016.07.003. Epub 2016 Jul 6.

PMID:
27498916
25.

Anti-D treatment for pediatric immune thrombocytopenia: Is the bad reputation justified?

Yacobovich J, Abu-Ahmed S, Steinberg-Shemer O, Goldberg T, Cohen M, Tamary H.

Semin Hematol. 2016 Apr;53 Suppl 1:S64-6. doi: 10.1053/j.seminhematol.2016.04.019. Epub 2016 Apr 8.

PMID:
27312170
26.

Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis.

Steinberg-Shemer O, Keel S, Dgany O, Walsh T, Noy-Lotan S, Krasnov T, Yacobovich J, Quarello P, Ramenghi U, King MC, Shimamura A, Tamary H.

J Pediatr Hematol Oncol. 2016 Oct;38(7):e260-2. doi: 10.1097/MPH.0000000000000587.

27.

Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I.

Shalev H, Al-Athamen K, Levi I, Levitas A, Tamary H.

Eur J Haematol. 2017 Jan;98(1):13-18. doi: 10.1111/ejh.12778. Epub 2016 Jun 15.

PMID:
27206021
28.

[BLUE BABY, PINK FUTURE].

Osovsky M, Yacobovich J, Sirota L, Tamary H.

Harefuah. 2016 Jan;155(1):24-6, 68. Hebrew.

PMID:
27012070
29.

Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia.

Gerrits AJ, Leven EA, Frelinger AL 3rd, Brigstocke SL, Berny-Lang MA, Mitchell WB, Revel-Vilk S, Tamary H, Carmichael SL, Barnard MR, Michelson AD, Bussel JB.

Blood. 2015 Sep 10;126(11):1367-78. doi: 10.1182/blood-2014-09-602573. Epub 2015 Jul 29.

30.

Triallelic and epigenetic-like inheritance in human disorders of telomerase.

Collopy LC, Walne AJ, Cardoso S, de la Fuente J, Mohamed M, Toriello H, Tamary H, Ling AJ, Lloyd T, Kassam R, Tummala H, Vulliamy TJ, Dokal I.

Blood. 2015 Jul 9;126(2):176-84. doi: 10.1182/blood-2015-03-633388. Epub 2015 May 29.

31.

Think about hemoglobinopathies.

Shemer OS, Tamary H.

Isr Med Assoc J. 2014 Dec;16(12):785-6. No abstract available.

32.

Patient and central venous catheter related risk factors for blood stream infections in children receiving chemotherapy.

Yacobovich J, Ben-Ami T, Abdalla T, Tamary H, Goldstein G, Weintraub M, Yaniv I, Toren A, Kenet G, Revel-Vilk S.

Pediatr Blood Cancer. 2015 Mar;62(3):471-6. doi: 10.1002/pbc.25281. Epub 2014 Oct 18.

PMID:
25327811
33.

Genetic analysis and clinical picture of severe congenital neutropenia in Israel.

Lebel A, Yacobovich J, Krasnov T, Koren A, Levin C, Kaplinsky C, Ravel-Vilk S, Laor R, Attias D, Ben Barak A, Shtager D, Stein J, Kuperman A, Miskin H, Dgany O, Giri N, Alter BP, Tamary H.

Pediatr Blood Cancer. 2015 Jan;62(1):103-8. doi: 10.1002/pbc.25251. Epub 2014 Oct 4.

PMID:
25284454
34.

Thalassemia major and sickle cell disease in adolescents and young adults.

Yacobovich J, Tamary H.

Acta Haematol. 2014;132(3-4):340-7. doi: 10.1159/000360235. Epub 2014 Sep 10. Review.

PMID:
25228560
35.

Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli Arabs.

Gilad O, Dgany O, Noy-Lotan S, Krasnov T, Elitzur S, Pissard S, Kventsel I, Yacobovich J, Tamary H.

Hemoglobin. 2014;38(5):319-24. doi: 10.3109/03630269.2014.954668. Epub 2014 Sep 15.

PMID:
25222045
36.

Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry.

Zeidler C, Grote UA, Nickel A, Brand B, Carlsson G, Cortesão E, Dufour C, Duhem C, Notheis G, Papadaki HA, Tamary H, Tjønnfjord GE, Tucci F, Van Droogenbroeck J, Vermylen C, Voglova J, Xicoy B, Welte K.

Haematologica. 2014 Aug;99(8):1395-402. doi: 10.3324/haematol.2013.099101. Epub 2014 Jul 4.

37.

Association between childhood nephrotic syndrome and hemophagocytic lymphohistiocytosis.

Landau D, Gurevich E, Kapelushnik J, Tamary H, Shelef I, Lazar I.

Pediatr Nephrol. 2013 Dec;28(12):2389-92. doi: 10.1007/s00467-013-2583-8. Epub 2013 Aug 15.

PMID:
23949593
38.

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.

Iolascon A, Heimpel H, Wahlin A, Tamary H.

Blood. 2013 Sep 26;122(13):2162-6. doi: 10.1182/blood-2013-05-468223. Epub 2013 Aug 12. Review.

39.

Age and duration of bleeding symptoms at diagnosis best predict resolution of childhood immune thrombocytopenia at 3, 6, and 12 months.

Revel-Vilk S, Yacobovich J, Frank S, Ben-Ami T, Yechieli M, Shkalim V, Lebel A, Semo-Oz R, Tamary H.

J Pediatr. 2013 Nov;163(5):1335-9.e1-2. doi: 10.1016/j.jpeds.2013.06.018. Epub 2013 Jul 25.

PMID:
23891349
40.

Childhood immune thrombocytopenia--who will spontaneously recover?

Yacobovich J, Revel-Vilk S, Tamary H.

Semin Hematol. 2013 Jan;50 Suppl 1:S71-4. doi: 10.1053/j.seminhematol.2013.03.013. Review.

41.

Small-platelet thrombocytopenia in a family with autosomal recessive inheritance pattern.

Levin C, Zalman L, Tamary H, Krasnov T, Khayat M, Shalev S, Salama I, Koren A.

Pediatr Blood Cancer. 2013 Oct;60(10):E128-30. doi: 10.1002/pbc.24581. Epub 2013 May 6.

PMID:
23650215
42.

MPL Baltimore mutation and thrombocytosis: case report and literature review.

Shkalim-Zemer V, Dgany O, Krasnov T, Yacobovich J, Tamary H.

J Pediatr Hematol Oncol. 2013 Apr;35(3):e112-4. doi: 10.1097/MPH.0b013e318286d54c. Review.

PMID:
23511495
43.

Anemia associated with acute infection in children: an animal model.

Ballin A, Hussein A, Vaknine H, Senecky Y, Avni Y, Schreiber L, Tamary H, Boaz M.

J Pediatr Hematol Oncol. 2013 Jan;35(1):14-7. doi: 10.1097/MPH.0b013e31827b12ab.

PMID:
23249959
44.

A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia.

Shalev H, Landau D, Pissard S, Krasnov T, Kapelushnik J, Gilad O, Broides A, Dgany O, Tamary H.

Eur J Haematol. 2013 Feb;90(2):127-33. doi: 10.1111/ejh.12047. Epub 2013 Jan 7.

PMID:
23206178
45.

High levels of soluble serum hemojuvelin in patients with congenital dyserythropoietic anemia type I.

Shalev H, Perez-Avraham G, Kapelushnik J, Levi I, Rabinovich A, Swinkels DW, Brasse-Lagnel C, Tamary H.

Eur J Haematol. 2013 Jan;90(1):31-6. doi: 10.1111/ejh.12027. Epub 2012 Dec 4.

PMID:
23095116
46.

From blood smear to lipid disorder: a case report.

Elitzur S, Yacobovich J, Dgany O, Krasnov T, Rosenbach Y, Tamary H.

J Pediatr Hematol Oncol. 2013 Nov;35(8):e329-31. doi: 10.1097/MPH.0b013e318271c915.

PMID:
23042024
47.

Spontaneous resolution of extreme thrombocytosis in 2 children.

Aviner S, Even-Or E, Tamary H.

Pediatr Hematol Oncol. 2012 May;29(4):372-7. doi: 10.3109/08880018.2012.662712.

PMID:
22568801
48.

Analysis of health-related quality of life in children with immune thrombocytopenia and their parents using the kids' ITP tools.

Zilber R, Bortz AP, Yacobovich J, Yaniv I, Tamary H.

J Pediatr Hematol Oncol. 2012 Jan;34(1):2-5. doi: 10.1097/MPH.0b013e3182329b4f.

PMID:
22215093
49.

Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group.

Kühne T, Berchtold W, Michaels LA, Wu R, Donato H, Espina B, Tamary H, Rodeghiero F, Chitlur M, Rischewski J, Imbach P; Intercontinental Cooperative ITP Study Group.

Haematologica. 2011 Dec;96(12):1831-7. doi: 10.3324/haematol.2011.050799. Epub 2011 Aug 31.

50.

Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population.

Russo R, Gambale A, Esposito MR, Serra ML, Troiano A, De Maggio I, Capasso M, Luzzatto L, Delaunay J, Tamary H, Iolascon A.

Am J Hematol. 2011 Sep;86(9):727-32. doi: 10.1002/ajh.22096.

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