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Items: 1 to 50 of 191

1.

Survival of patient with giant cell arteritis: Impact of vision loss and treatment with aspirin.

Nesher G, Poltorak V, Hindi I, Nesher R, Dror Y, Orbach H, Breuer GS.

Autoimmun Rev. 2019 Aug;18(8):831-834. doi: 10.1016/j.autrev.2019.06.003. Epub 2019 Jun 6. No abstract available.

PMID:
31176872
2.

Primed PMNs in healthy mouse and human circulation are first responders during acute inflammation.

Fine N, Barzilay O, Sun C, Wellappuli N, Tanwir F, Chadwick JW, Oveisi M, Tasevski N, Prescott D, Gargan M, Philpott DJ, Dror Y, Glogauer M.

Blood Adv. 2019 May 28;3(10):1622-1637. doi: 10.1182/bloodadvances.2018030585.

3.

PKD1L1-related situs inversus associated with sideroblastic anemia.

Rodriguez S, Chaturvedi R, Blanchette V, Dell S, Axford M, Cada M, Dror Y.

Clin Genet. 2019 May;95(5):629-630. doi: 10.1111/cge.13512. Epub 2019 Feb 21. No abstract available.

PMID:
30791085
4.

Sidedness Matters: Surrogate Biomarkers Prognosticate Colorectal Cancer upon Anatomic Location.

Ben-Aharon I, Goshen-Lago T, Sternschuss M, Morgenstern S, Geva R, Beny A, Dror Y, Steiner M, Hubert A, Idelevich E, Shulman K, Mishaeli M, Man S, Liebermann N, Soussan-Gutman L, Brenner B.

Oncologist. 2019 Aug;24(8):e696-e701. doi: 10.1634/theoncologist.2018-0351. Epub 2019 Feb 12.

PMID:
30755502
5.

Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and blood.

Shalata A, Lauhasurayotin S, Leibovitz Z, Li H, Hebert D, Dhanraj S, Hadid Y, Mahroum M, Bajar J, Egenburg S, Arad A, Shohat M, Haddad S, Bakry H, Moshiri H, Scherer SW, Tzur S, Dror Y.

J Med Genet. 2019 May;56(5):340-346. doi: 10.1136/jmedgenet-2018-105421. Epub 2018 Oct 16.

PMID:
30327448
6.

Understanding the evolving phenotype of vascular complications in telomere biology disorders.

Higgs C, Crow YJ, Adams DM, Chang E, Hayes D Jr, Herbig U, Huang JN, Himes R, Jajoo K, Johnson FB, Reynolds SD, Yonekawa Y, Armanios M, Boulad F, DiNardo CD, Dufour C, Goldman FD, Khan S, Kratz C, Myers KC, Raghu G, Alter BP, Aubert G, Bhala S, Cowen EW, Dror Y, El-Youssef M, Friedman B, Giri N, Helms Guba L, Khincha PP, Lin TF, Longhurst H, McReynolds LJ, Nelson A, Olson T, Pariser A, Perona R, Sasa G, Schratz K, Simonetto DA, Townsley D, Walsh M, Stevens K, Agarwal S, Bertuch AA, Savage SA; Clinical Care Consortium for Telomere-associated Ailments (CCCTAA).

Angiogenesis. 2019 Feb;22(1):95-102. doi: 10.1007/s10456-018-9640-7. Epub 2018 Aug 25.

PMID:
30168024
7.

Parkinson's disease phenotype is influenced by the severity of the mutations in the GBA gene.

Thaler A, Bregman N, Gurevich T, Shiner T, Dror Y, Zmira O, Gan-Or Z, Bar-Shira A, Gana-Weisz M, Orr-Urtreger A, Giladi N, Mirelman A.

Parkinsonism Relat Disord. 2018 Oct;55:45-49. doi: 10.1016/j.parkreldis.2018.05.009. Epub 2018 May 17.

PMID:
29784561
8.

ERCC6L2-associated inherited bone marrow failure syndrome.

Shabanova I, Cohen E, Cada M, Vincent A, Cohn RD, Dror Y.

Mol Genet Genomic Med. 2018 May;6(3):463-468. doi: 10.1002/mgg3.388. Epub 2018 Apr 6. Review.

9.

External validation of a collar-mounted triaxial accelerometer for second-by-second monitoring of eight behavioural states in dogs.

den Uijl I, Gómez Álvarez CB, Bartram D, Dror Y, Holland R, Cook A.

PLoS One. 2017 Nov 29;12(11):e0188481. doi: 10.1371/journal.pone.0188481. eCollection 2017.

10.

Molecular analysis and genotype-phenotype correlation of Diamond-Blackfan anemia.

Arbiv OA, Cuvelier G, Klaassen RJ, Fernandez CV, Robitaille N, Steele M, Breakey V, Abish S, Wu J, Sinha R, Silva M, Goodyear L, Jardine L, Lipton JH, Corriveau-Bourque C, Brossard J, Michon B, Ghemlas I, Waespe N, Zlateska B, Sung L, Cada M, Dror Y.

Clin Genet. 2018 Feb;93(2):320-328. doi: 10.1111/cge.13158. Epub 2017 Dec 27.

PMID:
29044489
11.

The clinical impact of copy number variants in inherited bone marrow failure syndromes.

Waespe N, Dhanraj S, Wahala M, Tsangaris E, Enbar T, Zlateska B, Li H, Klaassen RJ, Fernandez CV, Cuvelier GDE, Wu JK, Pastore YD, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Sinha R, Belletrutti MJ, Breakey VR, Jardine L, Goodyear L, Kofler L, Cada M, Sung L, Shago M, Scherer SW, Dror Y.

NPJ Genom Med. 2017 May 10;2. pii: 18. doi: 10.1038/s41525-017-0019-2.

12.

The effect of the serum corona on interactions between a single nano-object and a living cell.

Dror Y, Sorkin R, Brand G, Boubriak O, Urban J, Klein J.

Sci Rep. 2017 Apr 6;7:45758. doi: 10.1038/srep45758.

13.

Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.

Dhanraj S, Matveev A, Li H, Lauhasurayotin S, Jardine L, Cada M, Zlateska B, Tailor CS, Zhou J, Mendoza-Londono R, Vincent A, Durie PR, Scherer SW, Rommens JM, Heon E, Dror Y.

Blood. 2017 Mar 16;129(11):1557-1562. doi: 10.1182/blood-2016-08-735431. Epub 2017 Jan 6. No abstract available.

PMID:
28062395
14.

Moderate 'multivitamin' supplementation improved folate and vitamin B12 status in the elderly.

Tal S, Stern F, Polyak Z, Ichelzon I, Dror Y.

Exp Gerontol. 2016 Nov;84:101-106. doi: 10.1016/j.exger.2016.09.009. Epub 2016 Sep 9.

PMID:
27620820
15.

Underlying undiagnosed inherited marrow failure syndromes among children with cancer.

Alabbas F, Weitzman S, Grant R, Bouffet E, Malkin D, Abla O, Dror Y.

Pediatr Blood Cancer. 2017 Feb;64(2):302-305. doi: 10.1002/pbc.26120. Epub 2016 Aug 31.

PMID:
27577695
16.

Response to treatment with azacitidine in children with advanced myelodysplastic syndrome prior to hematopoietic stem cell transplantation.

Waespe N, Van Den Akker M, Klaassen RJ, Lieberman L, Irwin MS, Ali SS, Abdelhaleem M, Zlateska B, Liebman M, Cada M, Schechter T, Dror Y.

Haematologica. 2016 Dec;101(12):1508-1515. Epub 2016 Aug 18.

17.

Functional and Existential Tasks of Family Caregiving for End-of-Life, Hospitalized Older Adults.

Cohen CC, Auslander G, Dror YF, Breuer GS.

J Gerontol Nurs. 2016 Jul 1;42(7):55-64. doi: 10.3928/00989134-20160406-04. Epub 2016 Apr 11.

PMID:
27064609
18.

Case 1: A newborn with pancytopenia.

Cardona I, Ferretti E, Daboval T, Klaassen RJ, Dror Y.

Paediatr Child Health. 2016 Jan-Feb;21(1):9-11. No abstract available.

19.

Impact of the 12-Gene Colon Cancer Assay on Clinical Decision Making for Adjuvant Therapy in Stage II Colon Cancer Patients.

Brenner B, Geva R, Rothney M, Beny A, Dror Y, Steiner M, Hubert A, Idelevich E, Gluzman A, Purim O, Shacham-Shmueli E, Shulman K, Mishaeli M, Man S, Soussan-Gutman L, Tezcan H, Chao C, Shani A, Liebermann N.

Value Health. 2016 Jan;19(1):82-7. doi: 10.1016/j.jval.2015.08.013. Epub 2015 Oct 30.

20.

Distinct routes of lineage development reshape the human blood hierarchy across ontogeny.

Notta F, Zandi S, Takayama N, Dobson S, Gan OI, Wilson G, Kaufmann KB, McLeod J, Laurenti E, Dunant CF, McPherson JD, Stein LD, Dror Y, Dick JE.

Science. 2016 Jan 8;351(6269):aab2116. doi: 10.1126/science.aab2116. Epub 2015 Nov 5.

21.

Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN).

Dhanraj S, Gunja SM, Deveau AP, Nissbeck M, Boonyawat B, Coombs AJ, Renieri A, Mucciolo M, Marozza A, Buoni S, Turner L, Li H, Jarrar A, Sabanayagam M, Kirby M, Shago M, Pinto D, Berman JN, Scherer SW, Virtanen A, Dror Y.

J Med Genet. 2015 Nov;52(11):738-48. doi: 10.1136/jmedgenet-2015-103292. Epub 2015 Sep 4.

PMID:
26342108
22.

Response to comments from Drs. Alter and Rosenberg.

Dror Y, Cada M.

Haematologica. 2015 Sep;100(9):e381-2. doi: 10.3324/haematol.2015.130898. No abstract available.

23.

Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes.

Ghemlas I, Li H, Zlateska B, Klaassen R, Fernandez CV, Yanofsky RA, Wu J, Pastore Y, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Sinha R, Belletrutti M, Breakey VR, Jardine L, Goodyear L, Sung L, Dhanraj S, Reble E, Wagner A, Beyene J, Ray P, Meyn S, Cada M, Dror Y.

J Med Genet. 2015 Sep;52(9):575-84. doi: 10.1136/jmedgenet-2015-103270. Epub 2015 Jul 1.

PMID:
26136524
24.

Treatment of dyskeratosis congenita-associated pulmonary fibrosis with danazol.

Zlateska B, Ciccolini A, Dror Y.

Pediatr Pulmonol. 2015 Dec;50(12):E48-51. doi: 10.1002/ppul.23235. Epub 2015 Jun 17.

PMID:
26083318
25.

The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes.

Cada M, Segbefia CI, Klaassen R, Fernandez CV, Yanofsky RA, Wu J, Pastore Y, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Sinha R, Belletrutti M, Breakey V, Jardine L, Goodyear L, Sung L, Shago M, Beyene J, Sharma P, Zlateska B, Dror Y.

Haematologica. 2015 May;100(5):633-42. doi: 10.3324/haematol.2014.117457. Epub 2015 Feb 14.

26.

Vitamins in the prevention or delay of cognitive disability of aging.

Dror Y, Stern F, Gomori MJ.

Curr Aging Sci. 2014;7(3):187-213. Review.

PMID:
25643069
27.

Hair for brain trade-off, a metabolic bypass for encephalization.

Dror Y, Hopp M.

Springerplus. 2014 Sep 27;3:562. doi: 10.1186/2193-1801-3-562. eCollection 2014.

28.

Vitamin and mineral supplements in the primary prevention of cardiovascular disease and cancer.

Dror Y, Stern F.

Ann Intern Med. 2014 May 6;160(9):654. doi: 10.7326/L14-5009-2. No abstract available.

PMID:
24798531
29.

Mechanical stability and lubrication by phosphatidylcholine boundary layers in the vesicular and in the extended lamellar phases.

Sorkin R, Dror Y, Kampf N, Klein J.

Langmuir. 2014 May 6;30(17):5005-14. doi: 10.1021/la500420u. Epub 2014 Apr 22.

PMID:
24708462
30.

Transient erythroblastopenia of childhood is an underdiagnosed and self-limiting disease.

van den Akker M, Dror Y, Odame I.

Acta Paediatr. 2014 Jul;103(7):e288-94. doi: 10.1111/apa.12634. Epub 2014 Apr 29.

PMID:
24635829
31.

Protein products obtained by site-preferred partial crosslinking in protein crystals and "liberated" by redissolution.

Buch M, Wine Y, Dror Y, Rosenheck S, Lebendiker M, Giordano R, Leal RM, Popov AN, Freeman A, Frolow F.

Biotechnol Bioeng. 2014 Jul;111(7):1296-303. doi: 10.1002/bit.25186. Epub 2014 Jan 25.

PMID:
24420494
32.

Oral health comparison between children with neutropenia and healthy controls.

Park MS, Tenenbaum HC, Dror Y, Gloguaer M.

Spec Care Dentist. 2014 Jan-Feb;34(1):12-8. doi: 10.1111/j.1754-4505.2012.00299.x. Epub 2012 Nov 22.

PMID:
24382366
33.

Diagnosis and treatment of pediatric acquired aplastic anemia (AAA): an initial survey of the North American Pediatric Aplastic Anemia Consortium (NAPAAC).

Williams DA, Bennett C, Bertuch A, Bessler M, Coates T, Corey S, Dror Y, Huang J, Lipton J, Olson TS, Reiss UM, Rogers ZR, Sieff C, Vlachos A, Walkovich K, Wang W, Shimamura A.

Pediatr Blood Cancer. 2014 May;61(5):869-74. doi: 10.1002/pbc.24875. Epub 2013 Nov 27.

34.

Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopenia.

Boonyawat B, Dhanraj S, Al Abbas F, Zlateska B, Grunenbaum E, Roifman CM, Steele L, Meyn S, Blanchette V, Scherer SW, Swierczek S, Prchal J, Zhu Q, Torgerson TR, Ochs HD, Dror Y.

J Clin Immunol. 2013 Oct;33(7):1150-5. doi: 10.1007/s10875-013-9927-9. Epub 2013 Aug 14.

PMID:
23943155
35.

Origins of extreme boundary lubrication by phosphatidylcholine liposomes.

Sorkin R, Kampf N, Dror Y, Shimoni E, Klein J.

Biomaterials. 2013 Jul;34(22):5465-75. doi: 10.1016/j.biomaterials.2013.03.098. Epub 2013 Apr 23. Erratum in: Biomaterials. 2013 Dec;34(37):9637.

PMID:
23623226
36.

Vitamin D levels for preventing acute coronary syndrome and mortality: evidence of a nonlinear association.

Dror Y, Giveon SM, Hoshen M, Feldhamer I, Balicer RD, Feldman BS.

J Clin Endocrinol Metab. 2013 May;98(5):2160-7. doi: 10.1210/jc.2013-1185. Epub 2013 Mar 26.

PMID:
23533239
37.

Molecular characteristics of a pancreatic adenocarcinoma associated with Shwachman-Diamond syndrome.

Dhanraj S, Manji A, Pinto D, Scherer SW, Favre H, Loh ML, Chetty R, Wei AC, Dror Y.

Pediatr Blood Cancer. 2013 May;60(5):754-60. doi: 10.1002/pbc.24453. Epub 2013 Jan 9.

PMID:
23303473
38.

Reasons for choosing a career and workplace among occupational therapists and speech language pathologists.

Katz N, Gilad Izhaky S, Dror YF.

Work. 2013;45(3):343-8. doi: 10.3233/WOR-121532.

PMID:
23241700
39.

Long-ranged attraction between disordered heterogeneous surfaces.

Silbert G, Ben-Yaakov D, Dror Y, Perkin S, Kampf N, Klein J.

Phys Rev Lett. 2012 Oct 19;109(16):168305. Epub 2012 Oct 18.

PMID:
23215142
40.

Gray platelet syndrome: macrothrombocytopenia with deficient α-granules.

Kahr WH, Dror Y.

Blood. 2012 Sep 27;120(13):2543. No abstract available.

PMID:
23193541
41.

The relationship of sleep disturbance and symptom severity, symptom interference, and hospitalization among Israeli inpatients with cancer.

Monas L, Csorba S, Kovalyo M, Zeligman R, Dror YF, Musgrave CF.

Oncol Nurs Forum. 2012 Jul;39(4):E361-72. doi: 10.1188/12.ONF.E361-E372.

PMID:
22750907
42.

Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome.

Goh ES, Perez IC, Canales CP, Ruiz P, Agatep R, Yoon G, Chitayat D, Dror Y, Shago M, Goobie S, Sgro M, Walz K, Mendoza-Londono R.

Am J Med Genet A. 2012 Jul;158A(7):1579-88. doi: 10.1002/ajmg.a.35399. Epub 2012 May 25.

PMID:
22639462
43.

The impact of refeeding on blood fatty acids and amino acid profiles in elderly patients: a metabolomic analysis.

Dror Y, Almashanu S, Lubart E, Sela BA, Shimoni L, Segal R.

JPEN J Parenter Enteral Nutr. 2013 Jan;37(1):109-16. doi: 10.1177/0148607112443260. Epub 2012 Apr 6.

PMID:
22492466
44.

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome.

Dror Y, Donadieu J, Koglmeier J, Dodge J, Toiviainen-Salo S, Makitie O, Kerr E, Zeidler C, Shimamura A, Shah N, Cipolli M, Kuijpers T, Durie P, Rommens J, Siderius L, Liu JM.

Ann N Y Acad Sci. 2011 Dec;1242:40-55. doi: 10.1111/j.1749-6632.2011.06349.x.

PMID:
22191555
45.

The cellular and molecular mechanisms for neutropenia in Barth syndrome.

Makaryan V, Kulik W, Vaz FM, Allen C, Dror Y, Dale DC, Aprikyan AA.

Eur J Haematol. 2012 Mar;88(3):195-209. doi: 10.1111/j.1600-0609.2011.01725.x. Epub 2011 Dec 4.

46.

The ribosome-related protein, SBDS, is critical for normal erythropoiesis.

Sen S, Wang H, Nghiem CL, Zhou K, Yau J, Tailor CS, Irwin MS, Dror Y.

Blood. 2011 Dec 8;118(24):6407-17. doi: 10.1182/blood-2011-02-335190. Epub 2011 Sep 30.

PMID:
21963601
47.

Pain severity, satisfaction with pain management, and patient-related barriers to pain management in patients with cancer in Israel.

Naveh P, Leshem R, Dror YF, Musgrave CF.

Oncol Nurs Forum. 2011 Jul;38(4):E305-13. doi: 10.1188/11.ONF.E305-E313.

PMID:
21708526
48.

Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations.

Tsangaris E, Klaassen R, Fernandez CV, Yanofsky R, Shereck E, Champagne J, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Ali K, Dower N, Athale U, Jardine L, Hand JP, Odame I, Canning P, Allen C, Carcao M, Beyene J, Roifman CM, Dror Y.

J Med Genet. 2011 Sep;48(9):618-28. doi: 10.1136/jmg.2011.089821. Epub 2011 Jun 9. Erratum in: J Med Genet. 2012 Sep;49(9):597.

PMID:
21659346
49.

SBDS-deficiency results in deregulation of reactive oxygen species leading to increased cell death and decreased cell growth.

Ambekar C, Das B, Yeger H, Dror Y.

Pediatr Blood Cancer. 2010 Dec 1;55(6):1138-44. doi: 10.1002/pbc.22700.

PMID:
20979173
50.

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