Vol. 14 No. 3 (2013) | Egyptian Journal of Medical Human Genetics

Insight into Nek2A activity regulation and its pharmacological prospects

A Kumar, V Rajendran, R Sethumadhavan, R Purohit

213–219

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In silico profiling of miRNAs and their target polymorphisms in leukemia associated genes

CGP Doss, B Rajith, TSJ Seelan, RS Kumar

221–225

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Serum level of interleukin-10 with its gene polymorphism can be predictors of response to treatment in Egyptian patients with chronic hepatitis C virus

H El Bassat, LA Ali, RA Alm El-Din, E Hasby, A Shahbah

227–233

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Genotypic and phenotypic patterns of antimicrobial susceptibility of Helicobacter pylori strains among Egyptian patients

MS Fathi, RF EL-Folly, RA Hassan, ME El-Arab

235–246

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Does Caesalpinia bonducella ameliorate genotoxicity? An in vitro study in human lymphocyte culture and in vivo study in Albino mice

S Ahmad, S Ahmad, A Ali, M Afzal

247–257

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Conservative therapy versus intra-gastric balloon in treatment of Prader-Willi Syndrome morbid obesity

HN Ashem, SH Nagib, NS Thabet

259–265

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Possible association of interleukin-1beta (-511C/T) and interleukin-6 (-174G/C) gene polymorphisms with atherosclerosis in end stage renal disease Egyptian patients on maintenance haemodialysis

MH Kandil, GM Magour, GI Khalil, DA Maharem, AM Nomair

267–275

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Detection of bla SHV and bla CTX-M genes in ESBL producing Klebsiella pneumoniae isolated from Egyptian patients with suspected nosocomial infections

OI Ahmed, SA El-Hady, TM Ahmed, IZ Ahmed

277–283

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Comparative study: Parameters of gait in Down syndrome versus matched obese and healthy children

SA Elshemy

285–291

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Clinicolaboratory profile of phenylketonuria (PKU) in Sohag University Hospital-Upper Egypt

AA Sadek, AM Emam, MY Alhaggagy

293–298

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Effect of modified constrained induced movement therapy on improving arm function in children with obstetric brachial plexus injury

EM Abdel-Kafy, HM Kamal, SA Elshemy

299–305

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Assessment of immune function in Down syndrome patients

E Abdel-Salam, I Abdel-Meguid, S Korraa

307–310

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Oral-facial-digital syndrome type II: Transitional type between Mohr and Varadi

RM Shawky, SM Elsayed, HS Abd-Elkhalek, S Gad

311–315

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Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes in a Japanese child: Clinical, radiological and molecular genetic analysis

L Selim, D Mehaney

317–322

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Gastric sarcoidosis in children: A case report and review of the literature

SA Sadek, FA Elenin

323–325

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Basic concepts of medical genetics, Pathogenetics, Part 4: Anti-mutation mechanisms of the human genome and human proteome

MSZ Salem

327–330

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 14 No. 3 (2013) / Articles

Articles

Insight into Nek2A activity regulation and its pharmacological prospects

In silico profiling of miRNAs and their target polymorphisms in leukemia associated genes

Serum level of interleukin-10 with its gene polymorphism can be predictors of response to treatment in Egyptian patients with chronic hepatitis C virus

Genotypic and phenotypic patterns of antimicrobial susceptibility of Helicobacter pylori strains among Egyptian patients

Does Caesalpinia bonducella ameliorate genotoxicity? An in vitro study in human lymphocyte culture and in vivo study in Albino mice

Conservative therapy versus intra-gastric balloon in treatment of Prader-Willi Syndrome morbid obesity

Possible association of interleukin-1beta (-511C/T) and interleukin-6 (-174G/C) gene polymorphisms with atherosclerosis in end stage renal disease Egyptian patients on maintenance haemodialysis

Detection of bla SHV and bla CTX-M genes in ESBL producing Klebsiella pneumoniae isolated from Egyptian patients with suspected nosocomial infections

Comparative study: Parameters of gait in Down syndrome versus matched obese and healthy children

Clinicolaboratory profile of phenylketonuria (PKU) in Sohag University Hospital-Upper Egypt

Effect of modified constrained induced movement therapy on improving arm function in children with obstetric brachial plexus injury

Assessment of immune function in Down syndrome patients

Oral-facial-digital syndrome type II: Transitional type between Mohr and Varadi

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes in a Japanese child: Clinical, radiological and molecular genetic analysis

Gastric sarcoidosis in children: A case report and review of the literature

Basic concepts of medical genetics, Pathogenetics, Part 4: Anti-mutation mechanisms of the human genome and human proteome

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