Works matching AU John, Anne

Results: 51

Characterization of ACE2 naturally occurring missense variants: impact on subcellular localization and trafficking.

Published in:

Human Genomics, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s40246-022-00411-1

By:

Badawi, Sally;
Mohamed, Feda E.;
Alkhofash, Nesreen R.;
John, Anne;
Ali, Amanat;
Ali, Bassam R.

Publication type:

Article

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.

Published in:

Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0126-2

By:

Mitropoulos, Konstantinos;
Papadima, Eleni Merkouri;
Xiromerisiou, Georgia;
Balasopoulou, Angeliki;
Charalampidou, Kyriaki;
Galani, Vasiliki;
Zafeiri, Krystallia-Vassiliki;
Dardiotis, Efthymios;
Ralli, Styliani;
Deretzi, Georgia;
John, Anne;
Kydonopoulou, Kyriaki;
Papadopoulou, Elpida;
di Pardo, Alba;
Akcimen, Fulya;
Loizedda, Annalisa;
Dobričić, Valerija;
Novaković, Ivana;
Kostić, Vladimir S.;
Mizzi, Clint

Publication type:

Article

Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients.

Published in:

Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0120-8

By:

Chondrou, Vasiliki;
Kolovos, Petros;
Sgourou, Argyro;
Kourakli, Alexandra;
Pavlidaki, Alexia;
Kastrinou, Vlasia;
John, Anne;
Symeonidis, Argiris;
Ali, Bassam R.;
Papachatzopoulou, Adamantia;
Katsila, Theodora;
Patrinos, George P.

Publication type:

Article

Novel genetic risk variants for pediatric celiac disease.

Published in:

Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0091-1

By:

Balasopoulou, Angeliki;
Stanković, Biljana;
Panagiotara, Angeliki;
Nikčevic, Gordana;
Peters, Brock A.;
John, Anne;
Mendrinou, Effrosyni;
Stratopoulos, Apostolos;
Legaki, Aigli Ioanna;
Stathakopoulou, Vasiliki;
Tsolia, Aristoniki;
Govaris, Nikolaos;
Govari, Sofia;
Zagoriti, Zoi;
Poulas, Konstantinos;
Kanariou, Maria;
Constantinidou, Nikki;
Krini, Maro;
Spanou, Kleopatra;
Radlovic, Nedeljko

Publication type:

Article

Control of human immunodeficiency virus replication by cytotoxic T lymphocytes targeting subdominant epitopes.

Published in:

Nature Immunology, 2006, v. 7, n. 2, p. 173, doi. 10.1038/ni1281

By:

Frahm, Nicole;
Kiepiela, Photini;
Adams, Sharon;
Linde, Caitlyn H;
Hewitt, Hannah S;
Sango, Kaori;
Feeney, Margaret E;
Addo, Marylyn M;
Lichterfeld, Mathias;
Lahaie, Matthew P;
Pae, Eunice;
Wurcel, Alysse G;
Roach, Timothy;
St John, M Anne;
Altfeld, Marcus;
Marincola, Francesco M;
Moore, Corey;
Mallal, Simon;
Carrington, Mary;
Heckerman, David

Publication type:

Article

Effect of telerehabilitation on motor and functional outcomes in people with spinal cord injuries – a systematic review.

Published in:

European Journal of Physiotherapy, 2024, v. 26, n. 2, p. 95, doi. 10.1080/21679169.2023.2195439

By:

Nayak, Pradeepa;
John, Anne Mary;
Kaur, Parminder;
Mahmood, Amreen

Publication type:

Article

Impact of CYP3A4 and ABCB1 genetic variants on tacrolimus dosing in Greek kidney transplant recipients.

Published in:

Frontiers in Pharmacology, 2025, p. 1, doi. 10.3389/fphar.2025.1538432

By:

Tsironi, Anna;
Lazaros, Konstantinos;
Mendrinou, Effrosyni;
Papasotiriou, Marios;
Siamoglou, Stavroula;
Kydonopoulou, Kyriaki;
John, Anne;
Gerou, Alexandra;
Gerou, Spyridon;
Ali, Bassam R.;
Vrahatis, Aristidis G.;
Patrinos, George P.

Publication type:

Article

Retention in the endoplasmic reticulum is the underlying mechanism of some hereditary haemorrhagic telangiectasia type 2 ALK1 missense mutations.

Published in:

Molecular & Cellular Biochemistry, 2013, v. 373, n. 1/2, p. 247, doi. 10.1007/s11010-012-1496-3

By:

Hume, Alistair;
John, Anne;
Akawi, Nadia;
Al-Awadhi, Aydah;
Al-Suwaidi, Sarah;
Al-Gazali, Lihadh;
Ali, Bassam

Publication type:

Article

High tuberculosis and HIV coinfection rate, Johannesburg.

Published in:

2007

By:

John, Melanie-Anne;
Menezes, Colin Nigel;
Chita, Gajendra;
Sanne, Ian;
Grobusch, Martin Peter

Publication type:

Letter

Expression of Epstein-Barr virus in Hodgkin lymphoma in a population of United Arab Emirates nationals.

Published in:

Leukemia & Lymphoma, 2008, v. 49, n. 9, p. 1769, doi. 10.1080/10428190802270894

By:

Al-Salam, Suhail;
John, Anne;
Daoud, Sayel;
Chong, Siew Ming;
Castella, Antonio

Publication type:

Article

Bi‐allelic null variant in matrix metalloproteinase‐15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive.

Published in:

Clinical Genetics, 2022, v. 101, n. 4, p. 403, doi. 10.1111/cge.14107

By:

Abdelrahman, Hanadi A.;
Akawi, Nadia;
Al‐Shamsi, Aisha M.;
Ali, Amanat;
Al‐Jasmi, Fatma;
John, Anne;
Hertecant, Jozef;
Al‐Gazali, Lihadh;
Ali, Bassam R.

Publication type:

Article

Studies on N-Acetyltransferase (NAT2) Genotype Relationships in Emiratis: Confirmation of the Existence of Phenotype Variation among Slow Acetylators.

Published in:

Annals of Human Genetics, 2017, v. 81, n. 5, p. 190, doi. 10.1111/ahg.12198

By:

Al‐Ahmad, Mohammad M.;
Amir, Naheed;
Dhanasekaran, Subramanian;
John, Anne;
Abdulrazzaq, Yousef M.;
Ali, Bassam R.;
Bastaki, Salim

Publication type:

Article

GRP78/BiP alleviates oxLDL-induced hepatotoxicity in familial hypercholesterolemia caused by missense variants of LDLR in a HepG2 cellular model.

Published in:

Lipids in Health & Disease, 2023, v. 22, n. 1, p. 1, doi. 10.1186/s12944-023-01835-x

By:

Varghese, Divya Saro;
Oommen, Deepu;
John, Anne;
Ali, Bassam R.

Publication type:

Article

Cellular and functional evaluation of LDLR missense variants reported in hypercholesterolemic patients demonstrates their hypomorphic impacts on trafficking and LDL internalization.

Published in:

Frontiers in Cell & Developmental Biology, 2024, p. 1, doi. 10.3389/fcell.2024.1412236

By:

Jawabri, Aseel A.;
John, Anne;
Ghattas, Mohammad A.;
Mahgoub, Radwa E.;
Hamad, Mohammad I. K.;
Barakat, Maha T.;
Shobi, Bindu;
Daggag, Hinda;
Ali, Bassam R.

Publication type:

Article

Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome.

Published in:

Southern African Journal of Infectious Diseases, 2016, v. 31, n. 4, p. 119, doi. 10.1080/23120053.2016.1156874

By:

Manzini, Thandekile Cecilia;
Gosnell, Bernadett Isabel;
John, Melanie-Anne Amanda;
Moosa, Mahomed Yunus Suleman

Publication type:

Article

The stability of the boundary layer on a compliant rotating disc.

Published in:

IMA Journal of Applied Mathematics, 2007, v. 72, n. 6, p. 761, doi. 10.1093/imamat/hxm038

By:

John, Jo-Anne L.;
Stephen, Sharon O.

Publication type:

Article

Evaluation of Visual Outcomes of Cataract Surgery in Diabetic Patients and Assessment of Post-operative Complications as Compared to Non-diabetics.

Published in:

Journal of Clinical & Diagnostic Research, 2019, v. 13, n. 3, p. 10, doi. 10.7860/JCDR/2019/37529.12711

By:

SINGH, NEHA;
PAI, SHOBHA G.;
JOHN, TINA ANNE

Publication type:

Article

Clinical Profile of Congenital and Developmental Cataract in a Tertiary Care Centre of Southern India.

Published in:

Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 9, p. 1, doi. 10.7860/JCDR/2018/36080.11986

By:

KAMATH, SUMANA J.;
JOHN, TINA ANNE;
JAYANTHI, KALARY

Publication type:

Article

Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type in Turkish Patients Reveals a Novel Mutation and New Features.

Published in:

Molecular Syndromology, 2022, v. 13, n. 1, p. 23, doi. 10.1159/000517848

By:

Yilmaz Gulec, Elif;
Ali, Bassam R.;
John, Anne;
Tuysuz, Beyhan

Publication type:

Article

Further Delineation of the Microcephaly-Micromelia Syndrome Associated with Loss-of-Function Variants in DONSON.

Published in:

Molecular Syndromology, 2019, v. 10, n. 3, p. 171, doi. 10.1159/000497337

By:

abdelrahman, Hanadi a.;
John, anne;
ali, Bassam R.;
al-Gazali, Lihadh

Publication type:

Article

DNA methylation and repressive H3K9 and H3K27 trimethylation in the promoter regions of PD-1, CTLA-4, TIM-3, LAG-3, TIGIT, and PD-L1 genes in human primary breast cancer.

Published in:

Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0512-1

By:

Sasidharan Nair, Varun;
El Salhat, Haytham;
Taha, Rowaida Z.;
John, Anne;
Ali, Bassam R.;
Elkord, Eyad

Publication type:

Article

Hepatitis B immune reconstitution syndrome in a patient with HIV infection.

Published in:

International Journal of STD & AIDS, 2016, v. 27, n. 12, p. 1126, doi. 10.1177/0956462416628320

By:

John, Melanie-Anne A.;
Gosnell, Bernadett I.;
Manzini, Thandekile C.;
Ramdial, Prastistadevi;
Moosa, Mahomed-Yunus S.

Publication type:

Article

Hepatitis B immune reconstitution syndrome in a patient with HIV infection.

Published in:

2016

By:

John, Melanie-Anne A;
Gosnell, Bernadett I;
Manzini, Thandekile C;
Ramdial, Prastistadevi;
Moosa, Mahomed-Yunus S

Publication type:

journal article

Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population.

Published in:

Clinical Genetics, 1998, v. 54, n. 4, p. 285, doi. 10.1034/j.1399-0004.1998.5440405.x

By:

Frossard, Philippe M;
Hill, Susan H;
Elshahat, Yassin I;
Obineche, Eniyoma N;
Bokhari, Awais M;
Lestringant, Gilles G;
John, Anne;
Abdulle, Abdishakur M

Publication type:

Article

Genetic polymorphisms of cytochrome P450-1A2 (CYP1A2) among Emiratis.

Published in:

PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0183424

By:

Al-Ahmad, Mohammad M.;
Amir, Naheed;
Dhanasekaran, Subramanian;
John, Anne;
Abdulrazzaq, Yousef M.;
Ali, Bassam R.;
Bastaki, Salim M. A.

Publication type:

Article

Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum.

Published in:

Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1219514

By:

Kizhakkedath, Praseetha;
AlDhaheri, Watfa;
Baydoun, Ibrahim;
Tabouni, Mohammed;
John, Anne;
Almansoori, Taleb M.;
Al-Turki, Saeed;
Al-Jasmi, Fatma;
Alblooshi, Hiba

Publication type:

Article

Shaping the future-ready doctor: a first-aid kit to address a gap in medical education.

Published in:

International Journal of Medical Education, 2020, v. 11, p. 248, doi. 10.5116/ijme.5fad.2d3a

By:

Otaki, Farah;
Naidoo, Nerissa;
Al Heialy, Saba;
John-Baptiste, Anne-Marie;
Davis, Dave;
Senok, Abiola

Publication type:

Article

A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement.

Published in:

Orphanet Journal of Rare Diseases, 2016, v. 11, p. 1, doi. 10.1186/s13023-016-0526-8

By:

Akawi, Nadia A.;
Ben-Salem, Salma;
Hertecant, Jozef;
John, Anne;
Pramathan, Thachillath;
Kizhakkedath, Praseetha;
Ali, Bassam R.;
Al-Gazali, Lihadh

Publication type:

Article

Further Reduction in Mother-To-Child Transmission of HIV in Barbados following intervention with HAART.

Published in:

Journal of Eastern Caribbean Studies, 2011, v. 36, n. 4, p. 28

By:

St John, M. Anne;
Mascoll, Kemi;
Waterman, Ira;
Crichlow, Shawna

Publication type:

Article

A Novel SLC1A4 Mutation (p.Y191*) Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM) With Seizure Disorder.

Published in:

Child Neurology Open, 2019, v. 6, p. N.PAG, doi. 10.1177/2329048X19880647

By:

Abdelrahman, Hanadi A.;
Al-Shamsi, Aisha;
John, Anne;
Ali, Bassam R.;
Al-Gazali, Lihadh

Publication type:

Article

A Novel SLC1A4 Mutation (p.Y191*) Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM) With Seizure Disorder.

Published in:

Child Neurology Open, 2019, v. 6, n. 7, p. N.PAG, doi. 10.1177/2329048X19880647

By:

Abdelrahman, Hanadi A.;
Al-Shamsi, Aisha;
John, Anne;
Ali, Bassam R.;
Al-Gazali, Lihadh

Publication type:

Article

Spectrum of genetic variants in bilateral sensorineural hearing loss.

Published in:

Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1314535

By:

Ali, Amanat;
Tabouni, Mohammed;
Kizhakkedath, Praseetha;
Baydoun, Ibrahim;
Allam, Mushal;
John, Anne;
Busafared, Faiza;
Alnuaimi, Ayesha;
Al-Jasmi, Fatma;
Alblooshi, Hiba

Publication type:

Article

Captopril as a Potential Inhibitor of Lung Tumor Growth and Metastasis.

Published in:

Annals of the New York Academy of Sciences, 2008, v. 1138, p. 65, doi. 10.1196/annals.1414.011

By:

Attoub, Samir;
Gaben, Anne Marie;
Al‐Salam, Suhail;
Al Sultan, M.A.H.;
John, Anne;
Nicholls, M. Gary;
Mester, Jan;
Petroianu, Georg

Publication type:

Article

Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study.

Published in:

Hemoglobin, 2019, v. 43, n. 1, p. 27, doi. 10.1080/03630269.2019.1597732

By:

Kolliopoulou, Alexandra;
Siamoglou, Stavroula;
John, Anne;
Sgourou, Argyro;
Kourakli, Alexandra;
Symeonidis, Argiris;
Vlachaki, Efthymia;
Chalkia, Panagiota;
Theodoridou, Stamatia;
Ali, Bassam R.;
Katsila, Theodora;
Patrinos, George P.;
Papachatzopoulou, Adamantia

Publication type:

Article

Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemia.

Published in:

FEBS Open Bio, 2019, v. 9, n. 11, p. 1994, doi. 10.1002/2211-5463.12740

By:

Kizhakkedath, Praseetha;
John, Anne;
Al‐Sawafi, Buthaina K.;
Al‐Gazali, Lihadh;
Ali, Bassam R.

Publication type:

Article

A recessive truncating variant in thrombospondin‐1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous family.

Published in:

American Journal of Medical Genetics. Part A, 2018, v. 176, n. 9, p. 1996, doi. 10.1002/ajmg.a.40424

By:

Abdelrahman, Hanadi A.;
Al‐Shamsi, Aisha;
John, Anne;
Hertecant, Jozef;
Lootah, Ali;
Ali, Bassam R.;
Al‐Gazali, Lihadh

Publication type:

Article

A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing loss.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 5, p. 1257, doi. 10.1002/ajmg.a.38153

By:

Gariballa, Nesrin;
Ben‐Mahmoud, Afif;
Komara, Makanko;
Al‐Shamsi, Aisha M.;
John, Anne;
Ali, Bassam R.;
Al‐Gazali, Lihadh

Publication type:

Article

Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 2, p. 540, doi. 10.1002/ajmg.a.37421

By:

Komara, Makanko;
John, Anne;
Suleiman, Jehan;
Ali, Bassam R.;
Al‐Gazali, Lihadh

Publication type:

Article

Gonadal Mosaicism in ARID1B Gene Causes Intellectual Disability and Dysmorphic Features in Three Siblings.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 1, p. 156, doi. 10.1002/ajmg.a.37405

By:

Ben‐Salem, Salma;
Sobreira, Nara;
Akawi, Nadia A.;
Al‐Shamsi, Aisha M.;
John, Anne;
Pramathan, Thachillath;
Valle, David;
Ali, Bassam R.;
Al‐Gazali, Lihadh

Publication type:

Article

A Novel Whole Exon Deletion in WWOX Gene Causes Early Epilepsy, Intellectual Disability and Optic Atrophy.

Published in:

Journal of Molecular Neuroscience, 2015, v. 56, n. 1, p. 17, doi. 10.1007/s12031-014-0463-8

By:

Ben-Salem, Salma;
Al-Shamsi, Aisha;
John, Anne;
Ali, Bassam;
Al-Gazali, Lihadh

Publication type:

Article

Endoplasmic Reticulum Quality Control Is Involved in the Mechanism of Endoglin-Mediated Hereditary Haemorrhagic Telangiectasia.

Published in:

PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026206

By:

Ali, Bassam R.;
Ben-Rebeh, Imen;
John, Anne;
Akawi, Nadia A.;
Milhem, Reham M.;
Al-Shehhi, Nouf A.;
Al-Ameri, Mouza M.;
Al-Shamisi, Shamma A.;
Al-Gazali, Lihadh

Publication type:

Article

Unveiling the pathogenic mechanisms of NPR2 missense variants: insights into the genotype-associated severity in acromesomelic dysplasia and short stature.

Published in:

Frontiers in Cell & Developmental Biology, 2023, p. 1, doi. 10.3389/fcell.2023.1294748

By:

Badawi, Sally;
Varghese, Divya Saro;
Raj, Anjana;
John, Anne;
Al-Musafir, Hamda S.;
Al-Ghamari, Ahmed J.;
Alshamsi, Alreem R.;
Ouda, Sara H.;
Al-Dirbashi, Ghayth;
Ali, Bassam R.

Publication type:

Article

Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients.

Published in:

Genes, 2024, v. 15, n. 3, p. 309, doi. 10.3390/genes15030309

By:

Ivantsik, Ouliana;
John, Anne;
Kydonopoulou, Kyriaki;
Mitropoulos, Konstantinos;
Gerou, Spyridon;
Ali, Bassam R.;
Patrinos, George P.

Publication type:

Article

Emtricitabine-induced pure red cell aplasia.

Published in:

Southern African Journal of HIV Medicine, 2019, v. 20, n. 1, p. 1, doi. 10.4102/sajhivmed.v20i1.983

By:

Manickchund, Nithendra;
du Plessis, Camille;
John, Melanie-Anne A.;
Manzini, Thandekile C.;
Gosnell, Bernadett I.;
Lessells, Richard J.;
Moosa, Yunus S.

Publication type:

Article

Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report.

Published in:

2020

By:

Wong, Martin Ngie Liong;
Tang, Ing Ping;
Chor, Yek Kee;
Lau, Kiew Siong;
John, Anne Rachel;
Hii, King Ching;
Lee, Olive Pei Yi;
Lim, Wooi Kok;
Tan, Hannah Pei Koon

Publication type:

journal article

Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patients.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 11, p. 2239, doi. 10.1093/hmg/ddq103

By:

Ali, Bassam R.;
Xu, Huifang;
Akawi, Nadia A.;
John, Anne;
Karuvantevida, Noushad S.;
Langer, Ruth;
Al-Gazali, Lihadh;
Leitinger, Birgit

Publication type:

Article

Defective cellular trafficking of missense NPR-B mutants is the major mechanism underlying acromesomelic dysplasia-type Maroteaux.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 2, p. 267

By:

Hume, Alistair N.;
Buttgereit, Jens;
Al-Awadhi, Aydah M.;
Al-Suwaidi, Sarah S.;
John, Anne;
Bader, Michael;
Seabra, Miguel C.;
Al-Gazali, Lihadh;
Ali, Bassam R.

Publication type:

Article

Maximizing experiential co-curricular programs through Stakeholders' Theory: An explanatory mixed methods study.

Published in:

Journal of Experiential Education, 2022, v. 45, n. 4, p. 432, doi. 10.1177/10538259211073279

By:

Otaki, Farah;
Naidoo, Nerissa;
Al Heialy, Saba;
John-Baptiste, Anne-Marie;
Davis, Dave;
Senok, Abiola

Publication type:

Article

Leveraging the Added Value of Experiential Co-Curricular Programs to Humanize Medical Education.

Published in:

Journal of Experiential Education, 2022, v. 45, n. 2, p. 172, doi. 10.1177/10538259211021444

By:

Senok, Abiola;
John-Baptiste, Anne-Marie;
Al Heialy, Saba;
Naidoo, Nerissa;
Otaki, Farah;
Davis, Dave

Publication type:

Article

Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus.

Published in:

BMC Medical Genetics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12881-018-0540-x

By:

Al-Jezawi, Nesreen K.;
Al-Shamsi, Aisha M.;
Suleiman, Jehan;
Ben-Salem, Salma;
John, Anne;
Vijayan, Ranjit;
Ali, Bassam R.;
Al-Gazali, Lihadh

Publication type:

Article