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Items: 1 to 50 of 68

  • The following terms were not found in PubMed: Alumuku, Iordepuun.
1.

MTHFR polymorphisms as risk for male infertility in Pakistan and its comparison with socioeconomic status in the world.

Ullah N, Mansoor A, Micheal S, Mirza B, Qamar R, Mazhar K, Siddiqi S.

Per Med. 2019 Jan;16(1):35-49. doi: 10.2217/pme-2018-0045. Epub 2018 Nov 23.

PMID:
30468411
2.

Blended learning to teach gender in medical school.

Micheal S, Marjadi B.

Clin Teach. 2018 Jun;15(3):208-213. doi: 10.1111/tct.12778. Epub 2018 Apr 25.

PMID:
29696789
3.

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.

Micheal S, Niewold ITG, Siddiqui SN, Zafar SN, Khan MI, Bergen AAB.

Genes (Basel). 2018 Feb 20;9(2). pii: E112. doi: 10.3390/genes9020112.

4.

Attitudes of nurses towards care of the dying patient in India.

Lancaster RJ, Kautzmann C, Micheal JCJ, Chandrasekaran L, Jambunathan J, Chapin TM.

Int J Palliat Nurs. 2017 Nov 2;23(11):558-566. doi: 10.12968/ijpn.2017.23.11.558.

PMID:
29172892
5.

For the Love of the Game: Game- Versus Lecture-Based Learning With Generation Z Patients.

Adamson MA, Chen H, Kackley R, Micheal A.

J Psychosoc Nurs Ment Health Serv. 2018 Feb 1;56(2):29-36. doi: 10.3928/02793695-20171027-03. Epub 2017 Nov 8.

PMID:
29117424
6.

Variants in the PRPF8 Gene are Associated with Glaucoma.

Micheal S, Hogewind BF, Khan MI, Siddiqui SN, Zafar SN, Akhtar F, Qamar R, Hoyng CB, den Hollander AI.

Mol Neurobiol. 2018 May;55(5):4504-4510. doi: 10.1007/s12035-017-0673-5. Epub 2017 Jul 13.

7.

Persistent Left Superior Vena Cava in Fetuses: An Autopsy Series.

Ramakrishnan D, Chidambarathanu S, Murli L, Micheal J, Jagadeesh S, Suresh I, Seshadri S.

Fetal Pediatr Pathol. 2017 Aug;36(4):304-310. doi: 10.1080/15513815.2017.1324546. Epub 2017 Jun 1.

PMID:
28569558
8.

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Aung T, Ozaki M, Lee MC, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP Jr, Haripriya A, Williams SE, Astakhov YS, Orr AC, Burdon KP, Nakano S, Mori K, Abu-Amero K, Hauser M, Li Z, Prakadeeswari G, Bailey JNC, Cherecheanu AP, Kang JH, Nelson S, Hayashi K, Manabe SI, Kazama S, Zarnowski T, Inoue K, Irkec M, Coca-Prados M, Sugiyama K, Järvelä I, Schlottmann P, Lerner SF, Lamari H, Nilgün Y, Bikbov M, Park KH, Cha SC, Yamashiro K, Zenteno JC, Jonas JB, Kumar RS, Perera SA, Chan ASY, Kobakhidze N, George R, Vijaya L, Do T, Edward DP, de Juan Marcos L, Pakravan M, Moghimi S, Ideta R, Bach-Holm D, Kappelgaard P, Wirostko B, Thomas S, Gaston D, Bedard K, Greer WL, Yang Z, Chen X, Huang L, Sang J, Jia H, Jia L, Qiao C, Zhang H, Liu X, Zhao B, Wang YX, Xu L, Leruez S, Reynier P, Chichua G, Tabagari S, Uebe S, Zenkel M, Berner D, Mossböck G, Weisschuh N, Hoja U, Welge-Luessen UC, Mardin C, Founti P, Chatzikyriakidou A, Pappas T, Anastasopoulos E, Lambropoulos A, Ghosh A, Shetty R, Porporato N, Saravanan V, Venkatesh R, Shivkumar C, Kalpana N, Sarangapani S, Kanavi MR, Beni AN, Yazdani S, Lashay A, Naderifar H, Khatibi N, Fea A, Lavia C, Dallorto L, Rolle T, Frezzotti P, Paoli D, Salvi E, Manunta P, Mori Y, Miyata K, Higashide T, Chihara E, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Aihara M, Inatani M, Miyake M, Gotoh N, Matsuda F, Yoshimura N, Ikeda Y, Ueno M, Sotozono C, Jeoung JW, Sagong M, Park KH, Ahn J, Cruz-Aguilar M, Ezzouhairi SM, Rafei A, Chong YF, Ng XY, Goh SR, Chen Y, Yong VHK, Khan MI, Olawoye OO, Ashaye AO, Ugbede I, Onakoya A, Kizor-Akaraiwe N, Teekhasaenee C, Suwan Y, Supakontanasan W, Okeke S, Uche NJ, Asimadu I, Ayub H, Akhtar F, Kosior-Jarecka E, Lukasik U, Lischinsky I, Castro V, Grossmann RP, Sunaric Megevand G, Roy S, Dervan E, Silke E, Rao A, Sahay P, Fornero P, Cuello O, Sivori D, Zompa T, Mills RA, Souzeau E, Mitchell P, Wang JJ, Hewitt AW, Coote M, Crowston JG, Astakhov SY, Akopov EL, Emelyanov A, Vysochinskaya V, Kazakbaeva G, Fayzrakhmanov R, Al-Obeidan SA, Owaidhah O, Aljasim LA, Chowbay B, Foo JN, Soh RQ, Sim KS, Xie Z, Cheong AWO, Mok SQ, Soo HM, Chen XY, Peh SQ, Heng KK, Husain R, Ho SL, Hillmer AM, Cheng CY, Escudero-Domínguez FA, González-Sarmiento R, Martinon-Torres F, Salas A, Pathanapitoon K, Hansapinyo L, Wanichwecharugruang B, Kitnarong N, Sakuntabhai A, Nguyn HX, Nguyn GTT, Nguyn TV, Zenz W, Binder A, Klobassa DS, Hibberd ML, Davila S, Herms S, Nöthen MM, Moebus S, Rautenbach RM, Ziskind A, Carmichael TR, Ramsay M, Álvarez L, García M, González-Iglesias H, Rodríguez-Calvo PP, Fernández-Vega Cueto L, Oguz Ç, Tamcelik N, Atalay E, Batu B, Aktas D, Kasım B, Wilson MR, Coleman AL, Liu Y, Challa P, Herndon L, Kuchtey RW, Kuchtey J, Curtin K, Chaya CJ, Crandall A, Zangwill LM, Wong TY, Nakano M, Kinoshita S, den Hollander AI, Vesti E, Fingert JH, Lee RK, Sit AJ, Shingleton BJ, Wang N, Cusi D, Qamar R, Kraft P, Pericak-Vance MA, Raychaudhuri S, Heegaard S, Kivelä T, Reis A, Kruse FE, Weinreb RN, Pasquale LR, Haines JL, Thorsteinsdottir U, Jonasson F, Allingham RR, Milea D, Ritch R, Kubota T, Tashiro K, Vithana EN, Micheal S, Topouzis F, Craig JE, Dubina M, Sundaresan P, Stefansson K, Wiggs JL, Pasutto F, Khor CC.

Nat Genet. 2017 Jul;49(7):993-1004. doi: 10.1038/ng.3875. Epub 2017 May 29.

PMID:
28553957
9.

Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family.

Micheal S, Saksens NTM, Hogewind BF, Khan MI, Hoyng CB, den Hollander AI.

Mol Neurobiol. 2018 Feb;55(2):1387-1395. doi: 10.1007/s12035-017-0403-z. Epub 2017 Feb 1.

10.

Mercury concentration in muscle, bellyfat and liver from Oreochromis niloticus and Lates niloticus consumed in Lake Albert fishing communities in Uganda.

Andrew T, Francis E, Charles M, Naigaga I, Jessica N, Micheal O, Drago KC, Celsus S.

Cogent Food Agric. 2016 Dec 31;2(1):1214996. Epub 2016 Jul 22.

11.

Perceptions about mercury and lead in fish consumed in Lake Albert fishing communities Uganda.

Andrew T, Francis E, Charles M, Naigaga I, Jesca N, Micheal O, Anne K, Deborah A.

Cogent Food Agric. 2016 Dec 31;2(1):1220344. Epub 2016 Aug 17.

12.

Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.

Nikopoulos K, Farinelli P, Giangreco B, Tsika C, Royer-Bertrand B, Mbefo MK, Bedoni N, Kjellström U, El Zaoui I, Di Gioia SA, Balzano S, Cisarova K, Messina A, Decembrini S, Plainis S, Blazaki SV, Khan MI, Micheal S, Boldt K, Ueffing M, Moulin AP, Cremers FPM, Roepman R, Arsenijevic Y, Tsilimbaris MK, Andréasson S, Rivolta C.

Am J Hum Genet. 2016 Sep 1;99(3):770-776. doi: 10.1016/j.ajhg.2016.07.009.

13.

A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.

Micheal S, Siddiqui SN, Zafar SN, Villanueva-Mendoza C, Cortés-González V, Khan MI, den Hollander AI.

PLoS One. 2016 Jul 27;11(7):e0160016. doi: 10.1371/journal.pone.0160016. eCollection 2016.

14.

Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.

Micheal S, Siddiqui SN, Zafar SN, Iqbal A, Khan MI, den Hollander AI.

PLoS One. 2016 Jul 13;11(7):e0159259. doi: 10.1371/journal.pone.0159259. eCollection 2016.

15.

Neonatal Airway Obstruction from an Immature Teratoma: The Challenge of Appropriate Investigation in a Low-Resource Setting.

Abdallah Y, Micheal A.

Ann Med Health Sci Res. 2016 Jan-Feb;6(1):59-61. doi: 10.4103/2141-9248.180276.

16.

Safe emergency evacuation of a Tertiary Care Hospital during the "once in a century" floods in Chennai, India.

Kaliamoorthy I, Reddy MS, Rajakumar A, Varghese J, Pandey S, Pillai B, Micheal JC, Kancherla R, Rela M.

Indian J Crit Care Med. 2016 Feb;20(2):104-8. doi: 10.4103/0972-5229.175933.

17.

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.

Khor CC, Do T, Jia H, Nakano M, George R, Abu-Amero K, Duvesh R, Chen LJ, Li Z, Nongpiur ME, Perera SA, Qiao C, Wong HT, Sakai H, Barbosa de Melo M, Lee MC, Chan AS, Azhany Y, Dao TL, Ikeda Y, Perez-Grossmann RA, Zarnowski T, Day AC, Jonas JB, Tam PO, Tran TA, Ayub H, Akhtar F, Micheal S, Chew PT, Aljasim LA, Dada T, Luu TT, Awadalla MS, Kitnarong N, Wanichwecharungruang B, Aung YY, Mohamed-Noor J, Vijayan S, Sarangapani S, Husain R, Jap A, Baskaran M, Goh D, Su DH, Wang H, Yong VK, Yip LW, Trinh TB, Makornwattana M, Nguyen TT, Leuenberger EU, Park KH, Wiyogo WA, Kumar RS, Tello C, Kurimoto Y, Thapa SS, Pathanapitoon K, Salmon JF, Sohn YH, Fea A, Ozaki M, Lai JS, Tantisevi V, Khaing CC, Mizoguchi T, Nakano S, Kim CY, Tang G, Fan S, Wu R, Meng H, Nguyen TT, Tran TD, Ueno M, Martinez JM, Ramli N, Aung YM, Reyes RD, Vernon SA, Fang SK, Xie Z, Chen XY, Foo JN, Sim KS, Wong TT, Quek DT, Venkatesh R, Kavitha S, Krishnadas SR, Soumittra N, Shantha B, Lim BA, Ogle J, de Vasconcellos JP, Costa VP, Abe RY, de Souza BB, Sng CC, Aquino MC, Kosior-Jarecka E, Fong GB, Tamanaja VC, Fujita R, Jiang Y, Waseem N, Low S, Pham HN, Al-Shahwan S, Craven ER, Khan MI, Dada R, Mohanty K, Faiq MA, Hewitt AW, Burdon KP, Gan EH, Prutthipongsit A, Patthanathamrongkasem T, Catacutan MA, Felarca IR, Liao CS, Rusmayani E, Istiantoro VW, Consolandi G, Pignata G, Lavia C, Rojanapongpun P, Mangkornkanokpong L, Chansangpetch S, Chan JC, Choy BN, Shum JW, Than HM, Oo KT, Han AT, Yong VH, Ng XY, Goh SR, Chong YF, Hibberd ML, Seielstad M, Png E, Dunstan SJ, Chau NV, Bei J, Zeng YX, Karkey A, Basnyat B, Pasutto F, Paoli D, Frezzotti P, Wang JJ, Mitchell P, Fingert JH, Allingham RR, Hauser MA, Lim ST, Chew SH, Ebstein RP, Sakuntabhai A, Park KH, Ahn J, Boland G, Snippe H, Stead R, Quino R, Zaw SN, Lukasik U, Shetty R, Zahari M, Bae HW, Oo NL, Kubota T, Manassakorn A, Ho WL, Dallorto L, Hwang YH, Kiire CA, Kuroda M, Djamal ZE, Peregrino JI, Ghosh A, Jeoung JW, Hoan TS, Srisamran N, Sandragasu T, Set SH, Doan VH, Bhattacharya SS, Ho CL, Tan DT, Sihota R, Loon SC, Mori K, Kinoshita S, Hollander AI, Qamar R, Wang YX, Teo YY, Tai ES, Hartleben-Matkin C, Lozano-Giral D, Saw SM, Cheng CY, Zenteno JC, Pang CP, Bui HT, Hee O, Craig JE, Edward DP, Yonahara M, Neto JM, Guevara-Fujita ML, Xu L, Ritch R, Liza-Sharmini AT, Wong TY, Al-Obeidan S, Do NH, Sundaresan P, Tham CC, Foster PJ, Vijaya L, Tashiro K, Vithana EN, Wang N, Aung T.

Nat Genet. 2016 May;48(5):556-62. doi: 10.1038/ng.3540. Epub 2016 Apr 4.

PMID:
27064256
18.

Identification of Mutations in the PRDM5 Gene in Brittle Cornea Syndrome.

Micheal S, Khan MI, Islam F, Akhtar F, Qamar R, Tassignon MJ, Loeys B, den Hollander AI.

Cornea. 2016 Jun;35(6):853-9. doi: 10.1097/ICO.0000000000000824.

PMID:
27032025
19.

Blood lipids and prostate cancer: a Mendelian randomization analysis.

Bull CJ, Bonilla C, Holly JM, Perks CM, Davies N, Haycock P, Yu OH, Richards JB, Eeles R, Easton D, Kote-Jarai Z, Amin Al Olama A, Benlloch S, Muir K, Giles GG, MacInnis RJ, Wiklund F, Gronberg H, Haiman CA, Schleutker J, Nordestgaard BG, Travis RC, Neal D, Pashayan N, Khaw KT, Stanford JL, Blot WJ, Thibodeau S, Maier C, Kibel AS, Cybulski C, Cannon-Albright L, Brenner H, Park J, Kaneva R, Batra J, Teixeira MR, Micheal A, Pandha H, Smith GD, Lewis SJ, Martin RM; PRACTICAL consortium.

Cancer Med. 2016 Jun;5(6):1125-36. doi: 10.1002/cam4.695. Epub 2016 Mar 19.

20.

Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma.

Micheal S, Ayub H, Islam F, Siddiqui SN, Khan WA, Akhtar F, Qamar R, Khan MI, den Hollander AI.

PLoS One. 2015 Dec 29;10(12):e0145005. doi: 10.1371/journal.pone.0145005. eCollection 2015.

21.

Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndrome.

Micheal S, Siddiqui SN, Zafar SN, Venselaar H, Qamar R, Khan MI, den Hollander AI.

Neurogenetics. 2016 Jan;17(1):17-23. doi: 10.1007/s10048-015-0462-0. Epub 2015 Oct 21.

22.

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.

Maria M, Ajmal M, Azam M, Waheed NK, Siddiqui SN, Mustafa B, Ayub H, Ali L, Ahmad S, Micheal S, Hussain A, Shah ST, Ali SH, Ahmed W, Khan YM, den Hollander AI, Haer-Wigman L, Collin RW, Khan MI, Qamar R, Cremers FP.

PLoS One. 2015 Mar 16;10(3):e0119806. doi: 10.1371/journal.pone.0119806. eCollection 2015.

23.

Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts.

Micheal S, Ayub H, Khan MI, Bakker B, Schoenmaker-Koller FE, Ali M, Akhtar F, Khan WA, Qamar R, den Hollander AI.

Mol Vis. 2014 Nov 4;20:1471-9. eCollection 2014.

24.

CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia.

Badeeb OM, Micheal S, Koenekoop RK, den Hollander AI, Hedrawi MT.

BMC Med Genet. 2014 Sep 28;15:109. doi: 10.1186/s12881-014-0109-2.

25.

No lost opportunities in the emergency department.

Micheal JC.

Br J Nurs. 2014 Aug 12;23(15):830. doi: 10.12968/bjon.2014.23.15.830. No abstract available.

PMID:
25119322
26.

Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma.

Ayub H, Micheal S, Akhtar F, Khan MI, Bashir S, Waheed NK, Ali M, Schoenmaker-Koller FE, Shafique S, Qamar R, Hollander AI.

PLoS One. 2014 Aug 13;9(8):e105023. doi: 10.1371/journal.pone.0105023. eCollection 2014.

27.

Foil assisted replica molding for fabrication of microfluidic devices and their application in vitro.

Micheal IJ, Vidyasagar AJ, Bokara KK, Mekala NK, Asthana A, Rao ChM.

Lab Chip. 2014 Oct 7;14(19):3695-9. doi: 10.1039/c4lc00659c.

PMID:
25102283
28.

Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucoma.

Micheal S, Ayub H, Zafar SN, Bakker B, Ali M, Akhtar F, Islam F, Khan MI, Qamar R, den Hollander AI.

Clin Exp Ophthalmol. 2015 Jan-Feb;43(1):31-9. doi: 10.1111/ceo.12369. Epub 2014 Sep 23.

PMID:
25091052
29.

Surgical outcome and complications following cleft lip and palate repair in a teaching hospital in Nigeria.

Abdurrazaq TO, Micheal AO, Lanre AW, Olugbenga OM, Akin LL.

Afr J Paediatr Surg. 2013 Oct-Dec;10(4):345-57. doi: 10.4103/0189-6725.125447.

30.

Analyses of Sequence Variants in the MYOC Gene and of Single Nucleotide Polymorphisms in the NR3C1 and FKBP5 Genes in Corticosteroid-Induced Ocular Hypertension.

Hogewind BF, Micheal S, Schoenmaker-Koller FE, Hoyng CB, den Hollander AI.

Ophthalmic Genet. 2015;36(4):299-302. doi: 10.3109/13816810.2013.879598. Epub 2015 Aug 28.

PMID:
24417561
31.

Antioxidant enzymes as defense mechanism against oxidative stress in midgut tissue and hemocytes of Bombyx mori larvae subjected to various stressors.

Micheal AS, Subramanyam MV.

Arch Insect Biochem Physiol. 2013 Dec;84(4):222-34. doi: 10.1002/arch.21138. Epub 2013 Nov 12.

PMID:
24222080
32.

Immunoglobulin E reactivity and allergenic potency of Morus papyrifera (paper mulberry) pollen.

Micheal S, Wangorsch A, Wolfheimer S, Foetisch K, Minhas K, Scheurer S, Ahmed A.

J Investig Allergol Clin Immunol. 2013;23(3):168-75.

33.
34.

IL-4 gene polymorphisms and their association with atopic asthma and allergic rhinitis in Pakistani patients.

Micheal S, Minhas K, Ishaque M, Ahmed F, Ahmed A.

J Investig Allergol Clin Immunol. 2013;23(2):107-11.

35.

Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome.

Ajmal M, Khan MI, Neveling K, Tayyab A, Jaffar S, Sadeque A, Ayub H, Abbasi NM, Riaz M, Micheal S, Gilissen C, Ali SH, Azam M, Collin RW, Cremers FP, Qamar R.

Mol Vis. 2013;19:644-53. Epub 2013 Mar 21.

36.

Polymorphisms in matrix metalloproteinases MMP1 and MMP9 are associated with primary open-angle and angle closure glaucoma in a Pakistani population.

Micheal S, Yousaf S, Khan MI, Akhtar F, Islam F, Khan WA, den Hollander AI, Qamar R, Ahmed A.

Mol Vis. 2013;19:441-7. Epub 2013 Feb 20.

37.

Computational classification of mitochondrial shapes reflects stress and redox state.

Ahmad T, Aggarwal K, Pattnaik B, Mukherjee S, Sethi T, Tiwari BK, Kumar M, Micheal A, Mabalirajan U, Ghosh B, Sinha Roy S, Agrawal A.

Cell Death Dis. 2013 Jan 17;4:e461. doi: 10.1038/cddis.2012.213.

38.

Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan.

Khan MI, Ajmal M, Micheal S, Azam M, Hussain A, Shahzad A, Venselaar H, Bokhari H, de Wijs IJ, Hoefsloot LH, Waheed NK, Collin RW, den Hollander AI, Qamar R, Cremers FP.

Clin Genet. 2013 Sep;84(3):290-3. doi: 10.1111/cge.12039. Epub 2012 Nov 7. No abstract available.

PMID:
23134348
39.

Analysis of single nucleotide polymorphisms in the SFRS3 and FKBP4 genes in corticosteroid-induced ocular hypertension.

Hogewind BF, Micheal S, Bakker B, Hoyng CB, den Hollander AI.

Ophthalmic Genet. 2012 Dec;33(4):221-4. doi: 10.3109/13816810.2012.716488. Epub 2012 Aug 27.

PMID:
22921020
40.

Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndrome.

Micheal S, Khan MI, Akhtar F, Weiss MM, Islam F, Ali M, Qamar R, Maugeri A, den Hollander AI.

Mol Vis. 2012;18:1918-26. Epub 2012 Jul 18.

41.

Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa.

Ajmal M, Khan MI, Micheal S, Ahmed W, Shah A, Venselaar H, Bokhari H, Azam A, Waheed NK, Collin RW, den Hollander AI, Qamar R, Cremers FP.

Mol Vis. 2012;18:1226-37. Epub 2012 May 10.

42.

Role of Lysyl oxidase-like 1 gene polymorphisms in Pakistani patients with pseudoexfoliative glaucoma.

Micheal S, Khan MI, Akhtar F, Ali M, Ahmed A, den Hollander AI, Qamar R.

Mol Vis. 2012;18:1040-4. Epub 2012 Apr 25.

43.

Water ingestion affects orthostatic challenge-induced blood pressure and heart rate responses in young healthy subjects: gender implications.

Olatunji LA, Aaron AO, Micheal OS, Oyeyipo IP.

Niger J Physiol Sci. 2011 Nov 23;26(1):11-8.

PMID:
22314980
44.

Promoter polymorphisms of the CD14 gene are associated with atopy in Pakistani adults.

Micheal S, Minhas K, Ishaque M, Ahmed F, Ahmed A.

J Investig Allergol Clin Immunol. 2011;21(5):394-7.

45.

XRCC1 and XPD DNA repair gene polymorphisms: a potential risk factor for glaucoma in the Pakistani population.

Yousaf S, Khan MI, Micheal S, Akhtar F, Ali SH, Riaz M, Ali M, Lall P, Waheed NK, den Hollander AI, Ahmed A, Qamar R.

Mol Vis. 2011;17:1153-63. Epub 2011 May 4.

46.

Prevalence of skin test reactivity to aeroallergens in the Pakistani population.

Ahmed A, Minhas K, Micheal S, Ahmad F.

Public Health. 2011 May;125(5):324-6. doi: 10.1016/j.puhe.2011.02.005. Epub 2011 Apr 23.

PMID:
21524426
47.

Strong association between the -308 TNF promoter polymorphism and allergic rhinitis in Pakistani patients.

Minhas K, Micheal S, Ahmed F, Ahmed A.

J Investig Allergol Clin Immunol. 2010;20(7):563-6.

48.

Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa.

Khan MI, Collin RW, Arimadyo K, Micheal S, Azam M, Qureshi N, Faradz SM, den Hollander AI, Qamar R, Cremers FP.

Mol Vis. 2010 Dec 15;16:2753-9.

49.
50.

Nursing students' fingertips--is PDA a solution?

Venkatesaperumal R, Clara JJ, Raddaha AA, Venkatesaperumal S, Jambunathan J, Annitta E, Micheal IJ.

Nurs J India. 2010 Apr;101(4):89-92. No abstract available.

PMID:
21053667

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