Vol. 16 No. 1 (2015) | Egyptian Journal of Medical Human Genetics

Review- Cancer: Some genetic considerations

MSZ Salem

1-10

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Association of β-fibrinogen promoter gene polymorphism (148C/T), hyperfibrinogenemia and ischemic stroke in young adult patients

I Imran, R Lamsudin, P Idjradinata, TH Achmad, A Maskoen, S Wibowo, H Harapan

11-17

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Ankaferd Blood Stopper induces apoptosis and regulates PAR1 and EPCR expression in human leukemia cells

M Mumcuoglu, DF Akin, U Ezer, N Akar

19-27

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ACE DD genotype associated with the female Chronic Kidney Disease patients of Tamilnadu population

S Nagamani, MS Perumal, RLS Perumal, C Kesavan, K Muthusamy

29-33

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Apelin rs2235306 polymorphism is not related to metabolic syndrome in Egyptian women

ET Mehanna, DM Abo-Elmatty, MH Ghattas, NM Mesbah, SM Saleh

35-40

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Cytokeratin 18 as a non invasive marker in diagnosis of NASH and its usefulness in correlation with disease severity in Egyptian patients

MM Maher, WA Ibrahim, SA Saleh, L Shash, HA Gabal, M Tarif, M Gamal

41-46

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Fetal gender determination through Y-STR analysis of maternal plasma during the third trimester of pregnancy

HMH Aal-Hamdan, AM Refaat, SR Babu, AR Choudhry

47-53

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Effect of hand-arm bimanual intensive therapy on fine-motor performance in children with hemiplegic cerebral palsy

MAE Wahab, NES Hamed

55-59

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Some aspects of genetics and pharmacogenetics understanding by pharmacy students in Ukraine

OV Filiptsova, MN Kobets, YN Kobets

61-66

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Association between consanguinity and survival of marriages

M Saadat

67-70

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Frequency distribution of ABO and Rh (D) blood group alleles in Silte Zone, Ethiopia

K Tesfaye, Y Petros, M Andargie

71-76

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Effect of a new physical therapy concept on dynamic balance in children with spastic diplegic cerebral palsy

HAMAH Emara

77-83

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Editorial: Hardy–Weinberg disequilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

OM Hassanin

85-86

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Editorial: Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???

ME Kholy

87-88

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Case Report: Trichorhinophalangeal syndrome II, expanding the clinical spectrum

RM Shawky, HSA Elkhalek, AES Elghawaby, SA Mohammad, NS Seifeldin

89-94

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Case Report: Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes

MJ Marafie, IS Al Suliman, AM Redha, AM Alshati

95-99

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 16 No. 1 (2015) / Articles

Articles

Review- Cancer: Some genetic considerations

Association of β-fibrinogen promoter gene polymorphism (148C/T), hyperfibrinogenemia and ischemic stroke in young adult patients

Ankaferd Blood Stopper induces apoptosis and regulates PAR1 and EPCR expression in human leukemia cells

ACE DD genotype associated with the female Chronic Kidney Disease patients of Tamilnadu population

Apelin rs2235306 polymorphism is not related to metabolic syndrome in Egyptian women

Cytokeratin 18 as a non invasive marker in diagnosis of NASH and its usefulness in correlation with disease severity in Egyptian patients

Fetal gender determination through Y-STR analysis of maternal plasma during the third trimester of pregnancy

Effect of hand-arm bimanual intensive therapy on fine-motor performance in children with hemiplegic cerebral palsy

Some aspects of genetics and pharmacogenetics understanding by pharmacy students in Ukraine

Association between consanguinity and survival of marriages

Frequency distribution of ABO and Rh (D) blood group alleles in Silte Zone, Ethiopia

Effect of a new physical therapy concept on dynamic balance in children with spastic diplegic cerebral palsy

Editorial: Hardy–Weinberg disequilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

Editorial: Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???

Case Report: Trichorhinophalangeal syndrome II, expanding the clinical spectrum

Case Report: Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes

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