Works matching IS 11108630 AND DT 2018 AND VI 19 AND IP 4

Results: 25

Fuzzy system model for gene expression.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 301, doi. 10.1016/j.ejmhg.2018.06.002

By:

Sharma, Amit;
Adlakha, Neeru

Publication type:

Article

Impact of PAI-1 4G/5G and C > G polymorphisms in acute ST elevation myocardial infarction and stable angina patients: A single center Egyptian study.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 325, doi. 10.1016/j.ejmhg.2018.05.003

By:

Al-Wakeel, Hanan;
Sewelam, Nadia;
Khaled, Mohamed;
Abdelbar, Akram

Publication type:

Article

A study on the association of TCF7L2 rs11196205 (C/G) and CAPN10 rs3792267 (G/A) polymorphisms with type 2 diabetes mellitus in the South Western of Iran.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 403, doi. 10.1016/j.ejmhg.2018.01.007

By:

Gravand, Abdollah;
Foroughmand, Ali Mohammad;
Boroujeni, Mehdi Pourmehdi

Publication type:

Article

Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related cough.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 307, doi. 10.1016/j.ejmhg.2018.05.006

By:

Rohman, Mohammad Saifur;
Kuncahyo, Bagus Hery;
Yunita, Lowry;
Sidarta, Erdo Puncak;
Saka, Putu Nina Belinda;
Fajar, Jonny Karunia;
Heriansyah, Teuku;
Widodo, Nashi

Publication type:

Article

In silico analysis of the functional non-synonymous single nucleotide polymorphisms in the human CYP27B1 gene.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 367, doi. 10.1016/j.ejmhg.2018.03.001

By:

Rotimi, Solomon O.;
Peter, Olamide;
Oguntade, Oluwayomi;
Rotimi, Oluwakemi A.

Publication type:

Article

Cantu syndrome in an Egyptian child.

Published in:

2018

By:

Shawky, Rabah M.;
Gamal, Radwa

Publication type:

Case Study

Pathogenic predictions of non-synonymous variants and their impacts: A computational assessment of ARHGEF6 gene.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 333, doi. 10.1016/j.ejmhg.2018.05.002

By:

Khimsuriya, Yashvant M.;
Chauhan, Jenabhai B.

Publication type:

Article

MTHFR C677T polymorphism and risk of esophageal cancer: An updated meta-analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 273, doi. 10.1016/j.ejmhg.2018.04.003

By:

Kumar, Pradeep;
Rai, Vandana

Publication type:

Article

Metadherin mRNA expression in hepatocellular carcinoma.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 391, doi. 10.1016/j.ejmhg.2018.02.002

By:

Al-sheikh, Nevein M.;
El-Hefnway, Sally M.;
Abuamer, Ahmed M.;
Dala, Ashraf G.

Publication type:

Article

Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 353, doi. 10.1016/j.ejmhg.2018.04.005

By:

Ismail, Dina K.;
El-Tagui, Mona H.;
Hussein, Zeinab A.;
Eid, Mohamed A.;
Aly, Sobhy M.

Publication type:

Article

Helicobacter pylori Western cagA genotype in Egyptian patients with upper gastrointestinal disease.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 297, doi. 10.1016/j.ejmhg.2018.06.003

By:

Diab, Manal;
Gamal, Doaa;
El-Shenawy, Ahmed;
El-Sherbini, Effat;
Shemis, Mohamed;
Saber, Mohamed;
El-Ghannam, Maged

Publication type:

Article

Pathophysiology of bleeding diathesis in haemophilia-A: A sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic implications.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 285, doi. 10.1016/j.ejmhg.2018.01.003

By:

Ibrahim, Umma A.;
Ahmed, Sagir G.

Publication type:

Article

Detection of antimicrobial resistance genes of Helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 417, doi. 10.1016/j.ejmhg.2018.01.004

By:

Diab, Manal;
El-Shenawy, Ahmed;
Salem, Dalia;
El-Sherbini, Effat;
El-Ghannam, Maged;
Abdelnasser, Moustafa;
Abdel-Hady, Mahmoud;
Shaheen, Mohamed;
Saber, Mohamed

Publication type:

Article

FLT3 receptor/CD135 expression by flow cytometry in acute myeloid leukemia: Relation to FLT3 gene mutations and mRNA transcripts.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 345, doi. 10.1016/j.ejmhg.2018.04.006

By:

Mekawy, Mohamed Amin;
Eissa, Deena Samir;
Hamza, Mohamed Tarif;
Hamed, Gehan Mostafa;
Youssef, Mariam Karam

Publication type:

Article

Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 321, doi. 10.1016/j.ejmhg.2018.05.004

By:

Youssef, Omneya Ibrahim;
Raouf, Soha Youssef

Publication type:

Article

New insights into smudge cell percentage in chronic lymphocytic Leukemia: A novel prognostic indicator of disease burden.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 409, doi. 10.1016/j.ejmhg.2018.01.006

By:

Amal Abd El Hamid Mohamed;
Safwat, Nesma Ahmed

Publication type:

Article

Renalase gene polymorphisms (rs2576178 and rs10887800) in Egyptian hypertensive end stage renal disease patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 379, doi. 10.1016/j.ejmhg.2018.02.004

By:

Kandil, Noha S.;
El Sharkawy, Rania Mohamed;
Desouky, Lubna Mohamed Ibrahim;
Kandil, Lamia Said;
Masoud, I. M.;
Amin, Noha Gaber

Publication type:

Article

Study of DNA methyl transferase 3A mutation in acute myeloid leukemic patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 315, doi. 10.1016/j.ejmhg.2018.05.005

By:

Elsayed, Ghada M.;
Fahmi, Abd Elgawad A.;
Shafik, Nevine F.;
Elshimy, Reham A. A.;
Elhakeem, Heba K. Abd;
Attea, Sara A.

Publication type:

Article

Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion.

Published in:

2018

By:

Çelik, Vesile Deniz;
Kiliç, Betul Orhan;
Akis±in, Yasemin Ardiçoğlu;
Akar, Nejat;
Tükün, Fatma Ajlan

Publication type:

Case Study

Study of the role of IL-17F gene polymorphism in the development of immune thrombocytopenia among the Egyptian children.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 385, doi. 10.1016/j.ejmhg.2018.02.003

By:

Botros, Shahira K. A.;
Gad, Alaa A.;
Ibrahim, Ola M.

Publication type:

Article

The cephalofacial characterization in humans: The study using igbo tribe in Nigeria.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 399, doi. 10.1016/j.ejmhg.2018.02.001

By:

Sunday, Obaje Godwin;
Chinedu, Uzomba Godwin

Publication type:

Article

Genetic study of the NOTCH3 gene in CADASIL patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 425, doi. 10.1016/j.ejmhg.2018.05.001

By:

Chavoshi Tarzjani, Seyedeh Parisa;
Shahzadeh Fazeli, Seyed Abolhassan;
Sanati, Mohammad Hossein;
Mirzayee, Zahra

Publication type:

Article

Removal notice to "An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings" [Egypt J Med Hum Genet 18 (2017) 393-396].

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 443, doi. 10.1016/j.ejmhg.2018.04.004

By:

Elsayed, Solaf M.;
Gamal, Radwa

Publication type:

Article

The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report.

Published in:

2018

By:

Ozdemir, Ozturk;
Bourouba, Romyla;
Silan, Fatma;
Karakaya, Taner;
Yildiz, Onur;
Paksoy, Baris;
Urfali, Mine

Publication type:

Case Study

Study of congenital malformations in infants and children in Menoufia governorate, Egypt.

Published in:

Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 359, doi. 10.1016/j.ejmhg.2018.04.002

By:

AbouEl-Ella, Soheir S.;
Tawfik, Maha A.;
Abo El-Fotoh, Wafaa Moustafa M.;
Elbadawi, Mai A.

Publication type:

Article