Genetics

Eur Rev Med Pharmacol Sci 2022; 26 (16): 5983-5990
DOI: 10.26355/eurrev_202208_29540

Monkeypox: epidemiology, mode of transmission, clinical features, genetic clades and molecular properties

S. Kannan, P. Shaik Syed Ali, A. Sheeza
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Eur Rev Med Pharmacol Sci 2022; 26 (16): 5821-5828
DOI: 10.26355/eurrev_202208_29521

NLRP3 rs1539019 is significantly associated with chronic obstructive pulmonary disease in a Chinese Han population: a case-control study

Z.-F. Hou, Z.-H. Yuan, K. Chang, Y.-H. Cao, F.-X. Guan, Y. Gao
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Eur Rev Med Pharmacol Sci 2022; 26 (14): 5115-5127
DOI: 10.26355/eurrev_202207_29300

Mutational spectrum of the iduronate-2-sulfatase gene in Mexican patients with Hunter syndrome

M.A. Ramírez-Hernández, L.E. Figuera, L.C. Rizo-de la Torre, M.T. Magaña-Torres¸ S.C. Mendoza-Ruvalcaba, L. Arnaud-López, J.E. García-Ortiz, G.M. Zúñiga-González, A.M. Puebla-Pérez, B.C. Gómez-Meda, M.P. Gallegos-Arreola
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Eur Rev Med Pharmacol Sci 2022; 26 (14): 5107-5114
DOI: 10.26355/eurrev_202207_29298

Chest wall deformities and their possible associations with different genetic syndromes

N. Andreescu, A. Sharma, A. Mihailescu, C.G. Zimbru, V.L. David, R. Horhat, N.R. Kundnani, M. Puiu, S. Farcas
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Eur Rev Med Pharmacol Sci 2022; 26 (13): 4705-4708
DOI: 10.26355/eurrev_202207_29195

A novel ETV6-NTRK3 gene fusion in primary renal fibrosarcoma

H. Jiang
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Eur Rev Med Pharmacol Sci 2022; 26 (12): 4354-4366
DOI: 10.26355/eurrev_202206_29074

Association between CACNG2 polymorphisms (rs4820242, rs2284015 and rs2284017) and chronic peripheral neuropathic pain risk in a Mexican population

G.E. Mejía-Terrazas, E. López-Muñoz, A. Hidalgo-Bravo, M.G. Santamaria-Olmedo, M. Valdés-Flores
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Eur Rev Med Pharmacol Sci 2022; 26 (10): 3607-3620
DOI: 10.26355/eurrev_202205_28857

Identification of common key genes associated with Crohn’s Disease and IgA nephropathy

J. Yuan, Z. Wang, Y.-P. Wang
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Eur Rev Med Pharmacol Sci 2022; 26 (9): 3109-3126
DOI: 10.26355/eurrev_202205_28728

Potential genetic biomarker of Saudi Arabian patients with colorectal cancer

N.S. Younis, E.S. AlMasoud, F. Al Khawajah, F.J. Alghazal, H.M. AlMofarfesh, L.H. AL-Khalaf, M.S. Al Otaibi, S.M. Alkhamis, Z.A. Al Naser, Z.H. Al Mousa, Z.I. Alabdulaziz, M.E. Mohamed
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Eur Rev Med Pharmacol Sci 2022; 26 (7): 2437-2442
DOI: 10.26355/eurrev_202204_28478

Prader-Willi Syndrome and PCSK1 mutation: a novel presentation of combined syndromic and monogenic obesity

E. Kostopoulou, D.X. Spilioti, N.D. Pantzaris, B.E. Spiliotis
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Eur Rev Med Pharmacol Sci 2022; 26 (6): 2158-2164
DOI: 10.26355/eurrev_202203_28363

PPARα polymorphisms association with total cholesterol and LDL-C levels in a Mexican population

A.I. Ortega-Meléndez, S. Montero-Molina, R.F. Jiménez-Ortega, E. Ramírez-López, E. Campos-Góngora, R. Velázquez-Cruz, Z. Jiménez-Salas, I. Balderas-Rentería
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Eur Rev Med Pharmacol Sci 2022; 26 (6): 2143-2157
DOI: 10.26355/eurrev_202203_28362

Identification of epilepsy concomitant candidate genes recognized in Saudi epileptic patients

N.S. Younis, M.E. Mohamed, A.A. Alolayan, G.Y. Alhussain, H.A. Al-Mousa, J.A. Alshamrani, M.M. AlMutayib, M.M. AlQahtani, Z.A. Alhaddad, Z.S. Alfarhan, Z.A. AlOmran, M.M. Almostafa
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Eur Rev Med Pharmacol Sci 2022; 26 (5): 1475-1483
DOI: 10.26355/eurrev_202203_28211

Correlations of IL-18 and IL-6 gene polymorphisms and expression levels with onset of glioma

Y. Yang, Y.-J. Song, Q.-B. Nie, Y.-F. Wang, M. Zhang, G.-S. Mao
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Eur Rev Med Pharmacol Sci 2022; 26 (4): 1108-1113
DOI: 10.26355/eurrev_202202_28100

A novel presentation of an ATP1A3 gene mutation – case report and literature review

E. Kostopoulou, A. Avgeri, M.I. Apostolou, S. Tzifas, G. Dimitriou
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Eur Rev Med Pharmacol Sci 2021; 25 (22): 6881-6893
DOI: 10.26355/eurrev_202111_27236

CER 1 gene polymorphism in postmenopausal Roma and non-Roma Slovak women in connection with osteoporosis

M. Mydlárová Blaščáková, J. Mydlár, Z. Tomková, R. Hudáková, J. Poráčová, K. Hricová, M. Zigová, E. Petrejčíková, R. Omelka, M. Bauerová, A. Buriková, J. Vašková
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Eur Rev Med Pharmacol Sci 2021; 25 (17): 5463-5473
DOI: 10.26355/eurrev_202109_26655

The BDNF rs7934165 polymorphism is a biomarker of central obesity and cardiometabolic risk in Mexican women

I. Guerrero-Contreras, E.A. Hernández-Tobías, R.Velázquez-Cruz, E. Ramírez-López, E. Campos-Góngora, Z. Jiménez-Salas
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Eur Rev Med Pharmacol Sci 2021; 25 (7): 2949-2957
DOI: 10.26355/eurrev_202104_25548

7q35q36.3 deletion and concomitant 20q13.2q13.33 duplication in a newborn: familiar case

D. Dell’Edera, A. Allegretti, F. Forte, R.A. Dell’Edera, M.T. Dell’Edera, A.A. Epifania, L. Mercuri, C.R. Catacchio, A. Mitidieri, F. Simone, M. Ventura
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Eur Rev Med Pharmacol Sci 2021; 25 (3): 1447-1454
DOI: 10.26355/eurrev_202102_24852

A clinical characteristics and genetic analysis of a case of Rubinstein-Taybi syndrome with glaucoma

F.-R. Huang, A.-M. Zhang, J. Xu, L. Huang
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Eur Rev Med Pharmacol Sci 2021; 25 (1 Suppl): 33-42
DOI: 10.26355/eurrev_202112_27331

Improvement of quality of life by intake of hydroxytyrosol in patients with lymphedema and association of lymphedema genes with obesity

K. Dhuli, M.R. Ceccarini, V. Precone, P.E. Maltese, G. Bonetti, S. Paolacci, A. Dautaj, G. Guerri, G. Marceddu, T. Beccari, S. Michelini, M. Bertelli
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Eur Rev Med Pharmacol Sci 2021; 25 (1 Suppl): 14-22
DOI: 10.26355/eurrev_202112_27329

Genetics of fat deposition

G. Camilleri, A.K. Kiani, K.L. Herbst, J. Kaftalli, A. Bernini, K. Dhuli, E. Manara, G. Bonetti, L. Stuppia, S. Paolacci, A. Dautaj, M. Bertelli
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Eur Rev Med Pharmacol Sci 2020; 24 (23): 11998-12000
DOI: 10.26355/eurrev_202012_23987

Low-birth-weight infant with Antley-Bixler syndrome-like phenotype caused by POR mutation: a rare case report

G. Imataka, M. Fujisawa, R. Kuribayashi, G. Ichikawa, Y. Watabe, H. Suzumura, O. Arisaka, S. Yoshihara
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