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Items: 1 to 50 of 182

1.

Congenital Factor X deficiency in women: A systematic review of the literature.

Spiliopoulos D, Kadir RA.

Haemophilia. 2019 Mar;25(2):195-204. doi: 10.1111/hae.13729. Review.

PMID:
30901144
2.

SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome.

Wormser O, Gradstein L, Yogev Y, Perez Y, Kadir R, Goliand I, Sadka Y, El Riati S, Flusser H, Nachmias D, Birk R, Iraqi M, Kadar E, Gat R, Drabkin M, Halperin D, Horev A, Sivan S, Abdu U, Elia N, Birk OS.

Eur J Hum Genet. 2019 Feb 5. doi: 10.1038/s41431-019-0347-z. [Epub ahead of print]

PMID:
30723319
3.

Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish.

Perez Y, Bar-Yaacov R, Kadir R, Wormser O, Shelef I, Birk OS, Flusser H, Birnbaum RY.

Brain. 2019 Mar 1;142(3):574-585. doi: 10.1093/brain/awz004.

4.

Nocturnal Atrial Fibrillation Caused by Mutation in KCND2, Encoding Pore-Forming (α) Subunit of the Cardiac Kv4.2 Potassium Channel.

Drabkin M, Zilberberg N, Menahem S, Mulla W, Halperin D, Yogev Y, Wormser O, Perez Y, Kadir R, Etzion Y, Katz A, Birk OS.

Circ Genom Precis Med. 2018 Nov;11(11):e002293. doi: 10.1161/CIRCGEN.118.002293.

PMID:
30571183
5.

Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe.

Wormser O, Gradstein L, Kadar E, Yogev Y, Perez Y, Mashkit E, Elbedour K, Drabkin M, Markus B, Kadir R, Halperin D, Khalaila S, Levy J, Lifshitz T, Manor E, Birk OS.

Am J Med Genet A. 2018 Dec;176(12):2695-2703. doi: 10.1002/ajmg.a.40668. Epub 2018 Dec 4.

PMID:
30513137
6.

SEC31A mutation affects ER homeostasis, causing a neurological syndrome.

Halperin D, Kadir R, Perez Y, Drabkin M, Yogev Y, Wormser O, Berman EM, Eremenko E, Rotblat B, Shorer Z, Gradstein L, Shelef I, Birk R, Abdu U, Flusser H, Birk OS.

J Med Genet. 2019 Mar;56(3):139-148. doi: 10.1136/jmedgenet-2018-105503. Epub 2018 Nov 21.

PMID:
30464055
7.

Assessment of antibody assay methods in determination of prevalence of infectious bursal disease among local chickens and guinea fowls in Kwara state, North Central Nigeria.

Daodu OB, Oludairo OO, Aiyedun JO, Ambali HM, Kadir RA, Daodu OC, Olorunshola ID, Adah AD.

Vet World. 2018 Aug;11(8):1183-1187. doi: 10.14202/vetworld.2018.1183-1187. Epub 2018 Aug 28.

8.

A simple and inexpensive physical lysis method for DNA and RNA extraction from freshwater microalgae.

Yee W, Abdul-Kadir R, Lee LM, Koh B, Lee YS, Chan HY.

3 Biotech. 2018 Aug;8(8):354. doi: 10.1007/s13205-018-1381-1. Epub 2018 Aug 1.

PMID:
30105179
9.

Novel SBF1 splice-site null mutation broadens the clinical spectrum of Charcot-Marie-Tooth type 4B3 disease.

Flusser H, Halperin D, Kadir R, Shorer Z, Shelef I, Birk OS.

Clin Genet. 2018 Nov;94(5):473-479. doi: 10.1111/cge.13419. Epub 2018 Aug 9.

PMID:
30039846
10.

Impact and management of iron deficiency and iron deficiency anemia in women's health.

Mirza FG, Abdul-Kadir R, Breymann C, Fraser IS, Taher A.

Expert Rev Hematol. 2018 Sep;11(9):727-736. doi: 10.1080/17474086.2018.1502081. Epub 2018 Aug 1.

PMID:
30019973
11.

RSRC1 mutation affects intellect and behaviour through aberrant splicing and transcription, downregulating IGFBP3.

Perez Y, Menascu S, Cohen I, Kadir R, Basha O, Shorer Z, Romi H, Meiri G, Rabinski T, Ofir R, Yeger-Lotem E, Birk OS.

Brain. 2018 Apr 1;141(4):961-970. doi: 10.1093/brain/awy045.

PMID:
29522154
12.

Ligneous cervicitis and endometritis: A gynaecological presentation of congenital plasminogen deficiency.

Baithun M, Freeman-Wang T, Chowdary P, Kadir RA.

Haemophilia. 2018 May;24(3):359-365. doi: 10.1111/hae.13418. Epub 2018 Feb 13.

PMID:
29436075
13.

A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion.

Cohen I, Staretz-Chacham O, Wormser O, Perez Y, Saada A, Kadir R, Birk OS.

Am J Med Genet A. 2018 Feb;176(2):330-336. doi: 10.1002/ajmg.a.38574. Epub 2017 Dec 11.

PMID:
29226520
14.

European guidelines on perioperative venous thromboembolism prophylaxis: Surgery during pregnancy and the immediate postpartum period.

Ducloy-Bouthors AS, Baldini A, Abdul-Kadir R, Nizard J; ESA VTE Guidelines Task Force.

Eur J Anaesthesiol. 2018 Feb;35(2):130-133. doi: 10.1097/EJA.0000000000000704.

PMID:
29112543
15.

PAX7 mutation in a syndrome of failure to thrive, hypotonia, and global neurodevelopmental delay.

Proskorovski-Ohayon R, Kadir R, Michalowski A, Flusser H, Perez Y, Hershkovitz E, Sivan S, Birk OS.

Hum Mutat. 2017 Dec;38(12):1671-1683. doi: 10.1002/humu.23310. Epub 2017 Sep 22.

PMID:
28779497
16.

Iron deficiency across chronic inflammatory conditions: International expert opinion on definition, diagnosis, and management.

Cappellini MD, Comin-Colet J, de Francisco A, Dignass A, Doehner W, Lam CS, Macdougall IC, Rogler G, Camaschella C, Kadir R, Kassebaum NJ, Spahn DR, Taher AT, Musallam KM; IRON CORE Group.

Am J Hematol. 2017 Oct;92(10):1068-1078. doi: 10.1002/ajh.24820. Epub 2017 Jul 7. Review.

17.

Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers.

Hudecova I, Jiang P, Davies J, Lo YMD, Kadir RA, Chiu RWK.

Blood. 2017 Jul 20;130(3):340-347. doi: 10.1182/blood-2016-12-755017. Epub 2017 May 10.

18.

Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.

Yogev Y, Perez Y, Noyman I, Madegem AA, Flusser H, Shorer Z, Cohen E, Kachko L, Michaelovsky A, Birk R, Koifman A, Drabkin M, Wormser O, Halperin D, Kadir R, Birk OS.

Eur J Hum Genet. 2017 Aug;25(8):966-972. doi: 10.1038/ejhg.2017.85. Epub 2017 May 10.

19.

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders.

Orsini S, Noris P, Bury L, Heller PG, Santoro C, Kadir RA, Butta NC, Falcinelli E, Cid AR, Fabris F, Fouassier M, Miyazaki K, Lozano ML, Zúñiga P, Flaujac C, Podda GM, Bermejo N, Favier R, Henskens Y, De Maistre E, De Candia E, Mumford AD, Ozdemir GN, Eker I, Nurden P, Bayart S, Lambert MP, Bussel J, Zieger B, Tosetto A, Melazzini F, Glembotsky AC, Pecci A, Cattaneo M, Schlegel N, Gresele P; European Hematology Association - Scientific Working Group (EHA-SWG) on thrombocytopenias and platelet function disorders.

Haematologica. 2017 Jul;102(7):1192-1203. doi: 10.3324/haematol.2016.160754. Epub 2017 Apr 6.

20.

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome.

Perez Y, Shorer Z, Liani-Leibson K, Chabosseau P, Kadir R, Volodarsky M, Halperin D, Barber-Zucker S, Shalev H, Schreiber R, Gradstein L, Gurevich E, Zarivach R, Rutter GA, Landau D, Birk OS.

Brain. 2017 Apr 1;140(4):928-939. doi: 10.1093/brain/awx013.

21.

Heavy menstrual bleeding: An update on management.

Davies J, Kadir RA.

Thromb Res. 2017 Mar;151 Suppl 1:S70-S77. doi: 10.1016/S0049-3848(17)30072-5. Review.

PMID:
28262240
22.

Self-perceived mental well-being amongst Malaysian dentists.

Ab-Murat N, Mason L, Kadir RA, Yusoff N.

Int J Occup Saf Ergon. 2018 Jun;24(2):233-239. doi: 10.1080/10803548.2016.1268869. Epub 2017 Jan 9.

PMID:
28010176
23.

Enhancement of Hevea brasiliensis properties through chemical application.

Kadir R, Jantan MD.

An Acad Bras Cienc. 2016 Oct-Dec;88(4):2081-2092. doi: 10.1590/0001-3765201620150650.

24.

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases.

Hui WW, Jiang P, Tong YK, Lee WS, Cheng YK, New MI, Kadir RA, Chan KC, Leung TY, Lo YM, Chiu RW.

Clin Chem. 2017 Feb;63(2):513-524. doi: 10.1373/clinchem.2016.268375. Epub 2016 Dec 8.

25.

Mycobacterium smegmatis proteoliposome induce protection in a murine progressive pulmonary tuberculosis model.

Tirado Y, Puig A, Alvarez N, Borrero R, Aguilar A, Camacho F, Reyes F, Fernandez S, Perez JL, Acevedo R, Mata Espinoza D, Payan JA, Garcia ML, Kadir R, Sarmiento ME, Hernandez-Pando R, Norazmi MN, Acosta A.

Tuberculosis (Edinb). 2016 Dec;101:44-48. doi: 10.1016/j.tube.2016.07.017. Epub 2016 Aug 5.

PMID:
27865396
26.

Thrombosis and Hemostasis Related Issues in Women and Pregnancy.

Othman M, McLintock C, Kadir R.

Semin Thromb Hemost. 2016 Oct;42(7):693-695. Epub 2016 Oct 24. No abstract available.

PMID:
27776378
27.

Direct Oral Anticoagulants and Women.

Cohen H, Arachchillage DR, Beyer-Westendorf J, Middeldorp S, Kadir RA.

Semin Thromb Hemost. 2016 Oct;42(7):789-797. Epub 2016 Oct 5. Review.

PMID:
27706531
28.

The Management of Factor XI Deficiency in Pregnancy.

Davies J, Kadir R.

Semin Thromb Hemost. 2016 Oct;42(7):732-740. Epub 2016 Oct 3. Review.

PMID:
27699729
29.

PPARγ regulates exocrine pancreas lipase.

Danino H, Naor RP, Fogel C, Ben-Harosh Y, Kadir R, Salem H, Birk R.

Biochim Biophys Acta. 2016 Dec;1861(12 Pt A):1921-1928. doi: 10.1016/j.bbalip.2016.09.010. Epub 2016 Sep 20.

PMID:
27663184
30.

Plasma factor XIII level variations during menstrual cycle.

Sharief LA, Lawrie AS, Mackie IJ, Halimeh S, Kappert G, Smith C, Peyvandi F, Kadir RA.

Blood Coagul Fibrinolysis. 2016 Oct;27(7):786-790.

PMID:
27214035
31.

Management of direct oral anticoagulants in women of childbearing potential: guidance from the SSC of the ISTH: reply.

Cohen H, Arachchillage DR, Middeldorp S, Beyer-Westendorf J, Abdul-Kadir R.

J Thromb Haemost. 2017 Jan;15(1):195-197. doi: 10.1111/jth.13535. Epub 2016 Nov 25. No abstract available.

32.

Changes in thromboelastography parameters in pregnancy, labor, and the immediate postpartum period.

Shreeve NE, Barry JA, Deutsch LR, Gomez K, Kadir RA.

Int J Gynaecol Obstet. 2016 Sep;134(3):290-3. doi: 10.1016/j.ijgo.2016.03.010. Epub 2016 May 26.

PMID:
27451401
33.

Pregnancy outcome in patients exposed to direct oral anticoagulants - and the challenge of event reporting.

Beyer-Westendorf J, Michalski F, Tittl L, Middeldorp S, Cohen H, Abdul Kadir R, Arachchillage DJ, Arya R, Ay C, Marten S.

Thromb Haemost. 2016 Sep 27;116(4):651-8. doi: 10.1160/TH16-04-0305. Epub 2016 Jul 7.

PMID:
27384740
34.

Reduction of sodium content in spicy soups using monosodium glutamate.

Jinap S, Hajeb P, Karim R, Norliana S, Yibadatihan S, Abdul-Kadir R.

Food Nutr Res. 2016 Jun 27;60:30463. doi: 10.3402/fnr.v60.30463. eCollection 2016.

35.

Management of direct oral anticoagulants in women of childbearing potential: guidance from the SSC of the ISTH.

Cohen H, Arachchillage DR, Middeldorp S, Beyer-Westendorf J, Abdul-Kadir R.

J Thromb Haemost. 2016 Aug;14(8):1673-6. doi: 10.1111/jth.13366. Epub 2016 Jun 27. Review. No abstract available.

36.

Management of coagulopathy associated with postpartum hemorrhage: guidance from the SSC of the ISTH.

Collins P, Abdul-Kadir R, Thachil J; Subcommittees on Women' s Health Issues in Thrombosis and Haemostasis and on Disseminated Intravascular Coagulation.

J Thromb Haemost. 2016 Jan;14(1):205-10. doi: 10.1111/jth.13174. Epub 2015 Dec 23. No abstract available.

37.

ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size.

Kadir R, Harel T, Markus B, Perez Y, Bakhrat A, Cohen I, Volodarsky M, Feintsein-Linial M, Chervinski E, Zlotogora J, Sivan S, Birnbaum RY, Abdu U, Shalev S, Birk OS.

PLoS Genet. 2016 Mar 23;12(3):e1005919. doi: 10.1371/journal.pgen.1005919. eCollection 2016 Mar.

38.

UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN.

Perez Y, Kadir R, Volodarsky M, Noyman I, Flusser H, Shorer Z, Gradstein L, Birnbaum RY, Birk OS.

J Med Genet. 2016 Jun;53(6):397-402. doi: 10.1136/jmedgenet-2015-103352. Epub 2015 Nov 6.

PMID:
26545877
39.

The role of rotational thromboelastometry in assessment of haemostasis during pregnancy in women with factor XI deficiency.

Davies J, Harper A, Kadir RA.

Haemophilia. 2016 Mar;22(2):276-284. doi: 10.1111/hae.12807. Epub 2015 Nov 4.

PMID:
26538512
40.

Congenital factor V and VIII deficiency in women: a systematic review of literature and report of two new cases.

Spiliopoulos D, Kadir RA.

Blood Coagul Fibrinolysis. 2016 Apr;27(3):237-41. doi: 10.1097/MBC.0000000000000407. Review.

PMID:
26376169
41.

CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay.

Volodarsky M, Lichtig H, Leibson T, Sadaka Y, Kadir R, Perez Y, Liani-Leibson K, Gradstein L, Shaco-Levy R, Shorer Z, Frank D, Birk OS.

Hum Mol Genet. 2015 Nov 15;24(22):6485-91. doi: 10.1093/hmg/ddv357. Epub 2015 Sep 10.

PMID:
26358778
42.

Chemical compositions and termiticidal activities of the heartwood from Calophyllum inophyllum L.

Kadir R, Awang K, Khamaruddin Z, Soit Z.

An Acad Bras Cienc. 2015 Apr-Jun;87(2):743-51. doi: 10.1590/0001-3765201520140041.

43.

Mode of delivery and cranial bleeding in newborns with haemophilia: a systematic review and meta-analysis of the literature.

Davies J, Kadir RA.

Haemophilia. 2016 Jan;22(1):32-8. doi: 10.1111/hae.12726. Epub 2015 May 20. Review.

PMID:
25990680
44.

Thrombin generation assay identifies individual variability in responses to low molecular weight heparin in pregnancy: implications for anticoagulant monitoring.

Chowdary P, Adamidou D, Riddell A, Aghighi S, Griffioen A, Priest P, Moghadam L, Kelaher N, Huq FY, Kadir RA, Tuddenham EG, Gatt A.

Br J Haematol. 2015 Mar;168(5):719-27. doi: 10.1111/bjh.13193. Epub 2014 Oct 29.

PMID:
25351814
45.

Malaysia: empowering dentists into smoking cessation.

Nordin AS, Kadir RA.

Tob Control. 2014 Jul;23(4):284. No abstract available.

PMID:
25061647
46.

Empowering Malaysian dentists to tobacco dependence treatment conduct.

Nordin AS, Kadir RA, Yahya NA, Zakaria H, Rashid RA, Habil MH.

Int Dent J. 2014 Aug;64(4):206-12. doi: 10.1111/idj.12110. Epub 2014 May 19.

PMID:
24835463
47.

Evaluation and management of postpartum hemorrhage: consensus from an international expert panel.

Abdul-Kadir R, McLintock C, Ducloy AS, El-Refaey H, England A, Federici AB, Grotegut CA, Halimeh S, Herman JH, Hofer S, James AH, Kouides PA, Paidas MJ, Peyvandi F, Winikoff R.

Transfusion. 2014 Jul;54(7):1756-68. doi: 10.1111/trf.12550. Epub 2014 Mar 12. Erratum in: Transfusion. 2015 Mar;55(3):691.

PMID:
24617726
48.

VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2).

Feinstein M, Flusser H, Lerman-Sagie T, Ben-Zeev B, Lev D, Agamy O, Cohen I, Kadir R, Sivan S, Leshinsky-Silver E, Markus B, Birk OS.

J Med Genet. 2014 May;51(5):303-8. doi: 10.1136/jmedgenet-2013-101823. Epub 2014 Feb 27.

PMID:
24577744
49.

Changes in factor XIII level during pregnancy.

Sharief LT, Lawrie AS, Mackie IJ, Smith C, Peyvandi F, Kadir RA.

Haemophilia. 2014 Mar;20(2):e144-8. doi: 10.1111/hae.12345. Epub 2013 Dec 16.

PMID:
24329777
50.

Pregnancy complications and obstetric care in women with inherited bleeding disorders.

Kadir RA, Davies J, Winikoff R, Pollard D, Peyvandi F, Garagiola I, Pabinger I, Federici AB.

Haemophilia. 2013 Nov;19 Suppl 4:1-10. doi: 10.1111/hae.12269. Review.

PMID:
24102860

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