Búsqueda | BVS CLAP/SMR-OPS/OMS

1.

Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity.

Azman, Nurul Fatihah; Abdullah, Wan Zaidah; Hanafi, Sarifah; Diana, R; Bahar, Rosnah; Johan, Muhammad Farid; Zilfalil, Bin Alwi; Hassan, Rosline.

Ann Hematol ; 99(4): 729-735, 2020 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-32078010

2.

Ancestry-informative marker (AIM) SNP panel for the Malay population.

Yahya, Padillah; Sulong, Sarina; Harun, Azian; Wangkumhang, Pongsakorn; Wilantho, Alisa; Ngamphiw, Chumpol; Tongsima, Sissades; Zilfalil, Bin Alwi.

Int J Legal Med ; 134(1): 123-134, 2020 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-31760471

3.

Genotype-Phenotype Correlation of ß-Thalassemia in Malaysian Population: Toward Effective Genetic Counseling.

Abdullah, Uday Y H; Ibrahim, Hishamshah M; Mahmud, Noraesah Binti; Salleh, Mohamad Zaki; Teh, Lay Kek; Noorizhab, Mohd Nur Fakhruzzaman Bin; Zilfalil, Bin Alwi; Jassim, Haitham Muhammed; Wilairat, Prapin; Fucharoen, Suthat.

Hemoglobin ; 44(3): 184-189, 2020 May.

Artículo en Inglés | MEDLINE | ID: mdl-32586164

4.

Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, ß, Î³ and Î´ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in ß-Thalassemias.

Abdullah, Uday Y H; Ibrahim, Hishamshah M; Mahmud, Noraesah B; Salleh, Mohamad Z; Kek, Teh L; Noorizhab, Mohd N F B; Jassim, Haitham M; Othman, Iekhsan; Zainal Abidin, Syafiq A; Zilfalil, Bin Alwi; Wilairat, Prapin; Fucharoen, Suthat.

Hemoglobin ; 43(3): 182-187, 2019 May.

Artículo en Inglés | MEDLINE | ID: mdl-31298599

5.

Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies.

Hoh, Boon-Peng; Deng, Lian; Julia-Ashazila, Mat Jusoh; Zuraihan, Zakaria; Nur-Hasnah, Ma'amor; Nur-Shafawati, Ab Rajab; Hatin, Wan Isa; Endom, Ismail; Zilfalil, Bin Alwi; Khalid, Yusoff; Xu, Shuhua.

Hum Genomics ; 9: 16, 2015 Jul 22.

Artículo en Inglés | MEDLINE | ID: mdl-26194999

6.

The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies.

Kountouris, Petros; Stephanou, Coralea; Archer, Natasha; Bonifazi, Fedele; Giannuzzi, Viviana; Kuo, Kevin H M; Maggio, Aurelio; Makani, Julie; Mañú-Pereira, María Del Mar; Michailidou, Kyriaki; Nkya, Siana; Nnodu, Obiageli E; Trompeter, Sara; Tshilolo, Léon; Wonkam, Ambroise; Zilfalil, Bin Alwi; Inusa, Baba P D; Kleanthous, Marina.

Am J Hematol ; 96(11): E416-E420, 2021 11 01.

Artículo en Inglés | MEDLINE | ID: mdl-34406671

7.

The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia.

Deng, Lian; Hoh, Boon Peng; Lu, Dongsheng; Fu, Ruiqing; Phipps, Maude E; Li, Shilin; Nur-Shafawati, Ab Rajab; Hatin, Wan Isa; Ismail, Endom; Mokhtar, Siti Shuhada; Jin, Li; Zilfalil, Bin Alwi; Marshall, Christian R; Scherer, Stephen W; Al-Mulla, Fahd; Xu, Shuhua.

Hum Genet ; 133(9): 1169-85, 2014 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-24916469

8.

Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.

Rani, Abdul Qawee; Sasongko, Teguh Haryo; Sulong, Sarina; Bunyan, David; Salmi, Abdul Razak; Zilfalil, Bin Alwi; Matsuo, Masafumi; Zabidi-Hussin, Z A M H.

J Neurogenet ; 27(1-2): 11-5, 2013 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-23438214

9.

Molecular description of familial defective APOB-100 in Malaysia.

Al-Khateeb, Alyaa R; Mohd, Mohd Sapawi; Yusof, Zukarnai; Zilfalil, Bin Alwi.

Biochem Genet ; 51(9-10): 811-23, 2013 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-23775634

10.

Human Variome Project country nodes: documenting genetic information within a country.

Patrinos, George P; Smith, Timothy D; Howard, Heather; Al-Mulla, Fahd; Chouchane, Lotfi; Hadjisavvas, Andreas; Hamed, Sherifa A; Li, Xi-Tao; Marafie, Makia; Ramesar, Rajkumar S; Ramos, Feliciano J; de Ravel, Thomy; El-Ruby, Mona O; Shrestha, Tilak Ram; Sobrido, María-Jesús; Tadmouri, Ghazi; Witsch-Baumgartner, Martina; Zilfalil, Bin Alwi; Auerbach, Arleen D; Carpenter, Kevin; Cutting, Garry R; Dung, Vu Chi; Grody, Wayne; Hasler, Julia; Jorde, Lynn; Kaput, Jim; Macek, Milan; Matsubara, Yoichi; Padilla, Carmancita; Robinson, Helen; Rojas-Martinez, Augusto; Taylor, Graham R; Vihinen, Mauno; Weber, Tom; Burn, John; Qi, Ming; Cotton, Richard G H; Rimoin, David.

Hum Mutat ; 33(11): 1513-9, 2012 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-22753370

11.

Prevalence and Distribution of Major ß-Thalassemia Mutations and HbE/ß-Thalassemia Variant in Nepalese Ethnic Groups.

Lama, Raju; Yusof, Wardah; Shrestha, Tilak R; Hanafi, Sarifah; Bhattarai, Matrika; Hassan, Rosline; Zilfalil, Bin Alwi.

Hematol Oncol Stem Cell Ther ; 15(1): 14-20, 2022 Mar 01.

Artículo en Inglés | MEDLINE | ID: mdl-33592169

12.

Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2 and HBB associated with haemoglobinopathies.

Tamana, Stella; Xenophontos, Maria; Minaidou, Anna; Stephanou, Coralea; Harteveld, Cornelis L; Bento, Celeste; Traeger-Synodinos, Joanne; Fylaktou, Irene; Yasin, Norafiza Mohd; Abdul Hamid, Faidatul Syazlin; Esa, Ezalia; Halim-Fikri, Hashim; Zilfalil, Bin Alwi; Kakouri, Andrea C; Kleanthous, Marina; Kountouris, Petros.

Elife ; 112022 Dec 01.

Artículo en Inglés | MEDLINE | ID: mdl-36453528

13.

Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries.

Halim-Fikri, Bin Hashim; Lederer, Carsten W; Baig, Atif Amin; Mat-Ghani, Siti Nor Assyuhada; Syed-Hassan, Sharifah-Nany Rahayu-Karmilla; Yusof, Wardah; Abdul Rashid, Diana; Azman, Nurul Fatihah; Fucharoen, Suthat; Panigoro, Ramdan; Silao, Catherine Lynn T; Viprakasit, Vip; Jalil, Norunaluwar; Mohd Yasin, Norafiza; Bahar, Rosnah; Selvaratnam, Veena; Mohamad, Norsarwany; Nik Hassan, Nik Norliza; Esa, Ezalia; Krause, Amanda; Robinson, Helen; Hasler, Julia; Stephanou, Coralea; Raja-Sabudin, Raja-Zahratul-Azma; Elion, Jacques; El-Kamah, Ghada; Coviello, Domenico; Yusoff, Narazah; Abdul Latiff, Zarina; Arnold, Chris; Burn, John; Kountouris, Petros; Kleanthous, Marina; Ramesar, Raj; Zilfalil, Bin Alwi.

J Pers Med ; 12(4)2022 Mar 31.

Artículo en Inglés | MEDLINE | ID: mdl-35455667

14.

Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.

Rani, Abdul Qawee; Malueka, Rusdy Ghazali; Sasongko, Teguh Haryo; Awano, Hiroyuki; Lee, Tomoko; Yagi, Mariko; Zilfalil, Bin Alwi; Salmi, A B Razak; Takeshima, Yasuhiro; Zabidi-Hussin, Z A M H; Matsuo, Masafumi.

Mol Genet Metab ; 103(3): 303-4, 2011 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-21514860

15.

Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population.

Salahshourifar, Iman; Halim, Ahmad Sukari; Wan Sulaiman, Wan Azman; Zilfalil, Bin Alwi.

J Hum Genet ; 56(11): 755-8, 2011 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-21866112

16.

Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.

Sasongko, Teguh Haryo; Zilfalil, Bin Alwi; Zabidi-Hussin, Zamh.

J Neurogenet ; 25(1-2): 15-6, 2011 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-21338334

17.

Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population.

Salahshourifar, Iman; Sulaiman, Wan Azman Wan; Zilfalil, Bin Alwi; Halim, Ahmad Sukari.

Am J Med Genet A ; 155A(9): 2302-7, 2011 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-21834040

18.

The Role of Genetic Pathways in the Development of Chemoradiation Resistance in Nasopharyngeal Carcinoma (NPC) Patients.

Mat Lazim, Norhafiza; Che Lah, Che Ismail; Wan Juhari, Wan Khairunnisa; Sulong, Sarina; Zilfalil, Bin Alwi; Abdullah, Baharudin.

Genes (Basel) ; 12(11)2021 11 21.

Artículo en Inglés | MEDLINE | ID: mdl-34828441

19.

Whole-Genome Profiles of Malay Colorectal Cancer Patients with Intact MMR Proteins.

Juhari, Wan Khairunnisa Wan; Ahmad Amin Noordin, Khairul Bariah; Zakaria, Andee Dzulkarnaen; Rahman, Wan Faiziah Wan Abdul; Mokhter, Wan Muhamad Mokhzani Wan Muhamad; Hassan, Muhammad Radzi Abu; Sidek, Ahmad Shanwani Mohammed; Zilfalil, Bin Alwi.

Genes (Basel) ; 12(9)2021 09 20.

Artículo en Inglés | MEDLINE | ID: mdl-34573430

20.

Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate.

Salahshourifar, Iman; Halim, Ahmad Sukari; Sulaiman, Wan Azman Wan; Zilfalil, Bin Alwi.

Am J Med Genet A ; 152A(7): 1818-21, 2010 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-20583164

BVS CLAP/SMR-OPS/OMS

Centro Latinoamericano de Perinatología, Salud de la Mujer y Reproductiva

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