Vol. 12 No. 2 (2011) | Egyptian Journal of Medical Human Genetics

Published: 2012-03-12

Models to explore the molecular function and regulation of AIRE

T Lovewell, R Tazi-Ahnini

107-115

DOI:

10.1016/j.ejmhg.2011.06.008

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Hereditary periodic fever syndromes

RM Shawky, NEA Gaboon

117-125

DOI:

10.1016/j.ejmhg.2011.07.005

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Correlation between the RhD genotyping and RhD serotyping in isoimmunized pregnancies

SM Nour El Din, ARM ARamy, MS Ali

127-133

DOI:

10.1016/j.ejmhg.2011.06.005

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Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects

D Torun, E Yılmaz, E Akar, N Akar

135-137

DOI:

10.1016/j.ejmhg.2011.06.006

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Serum interferon-alpha level in first degree relatives of systemic lupus erythematosus patients: Correlation with autoantibodies titers

D Shahin, AM El-Refaey, AK El-Hawary, AA Salam, S Machaly, N Abousamra, RM El-farahaty

139-146

DOI:

10.1016/j.ejmhg.2011.06.009

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Low bone density management via capacitively coupled electrical fields and low intensity pulsed ultrasound in hemiparetic cerebral palsy

KA Olama

147-150

DOI:

10.1016/j.ejmhg.2011.06.003

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Genetic association between common beta-2 adrenoreceptor polymorphism and asthma severity in school-age children

MS Salama, NA Ashaat, AA Hamad

151-156

DOI:

10.1016/j.ejmhg.2011.07.003

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Consanguineous matings among Egyptian population

RM Shawky, MY El-Awady, SM Elsayed, GE Hamadan

157-163

DOI:

10.1016/j.ejmhg.2011.07.001

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Serine protease (TPS): A diagnostic and prognostic marker in pediatric patients with acute non-lymphoblastic leukemia

SHA Agwa, NS El-Kinawy, AA Shuoyb

165-170

DOI:

10.1016/j.ejmhg.2011.07.004

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Ocular features in Egyptian genetically disabled children

GR El-Hawary, RM Shawky, AS El-Din, SMN El-Din

171-181

DOI:

10.1016/j.ejmhg.2011.06.004

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Thiopurine S-methyltransferase genetic polymorphism in the Tunisian population

LB Salah, CB Salem, F B’Chir, K Bouraoui, F Broly, S Saguem

183-186

DOI:

10.1016/j.ejmhg.2011.08.004

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Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population

NA Elhawary, N Bogari, M Rashad, MT Tayeb

187-192

DOI:

10.1016/j.ejmhg.2011.07.008

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Endurance exercises versus treadmill training in improving muscle strength and functional activities in hemiparetic cerebral palsy

KA Olama

193-199

DOI:

10.1016/j.ejmhg.2011.07.002

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Molecular detection of circulating thyroid specific transcripts (TSHR/Tg-mRNAs) in thyroid cancer patients: Their diagnostic significance

SH Teama, SHA Agwa, A Fawzy, MM Sayed, WA Ibrahim, YM Eid

201-209

DOI:

10.1016/j.ejmhg.2011.08.002

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Salivary PCR detection of Helicobacter pylori DNA in Egyptian patients with dyspepsia

MM Sayed, WA Ibrahim, SA Abdel-bary, SM Abdelhakam, SA El-Masry, D Ghoraba

211-216

DOI:

10.1016/j.ejmhg.2011.08.003

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Goldenhar syndrome with skin tags on the chest wall

RM Shawky, SS Zahra

217-220

DOI:

10.1016/j.ejmhg.2011.06.001

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 12 No. 2 (2011) / Articles

Articles

Models to explore the molecular function and regulation of AIRE

DOI:

Hereditary periodic fever syndromes

DOI:

Correlation between the RhD genotyping and RhD serotyping in isoimmunized pregnancies

DOI:

Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects

DOI:

Serum interferon-alpha level in first degree relatives of systemic lupus erythematosus patients: Correlation with autoantibodies titers

DOI:

Low bone density management via capacitively coupled electrical fields and low intensity pulsed ultrasound in hemiparetic cerebral palsy

DOI:

Genetic association between common beta-2 adrenoreceptor polymorphism and asthma severity in school-age children

DOI:

Consanguineous matings among Egyptian population

DOI:

Serine protease (TPS): A diagnostic and prognostic marker in pediatric patients with acute non-lymphoblastic leukemia

DOI:

Ocular features in Egyptian genetically disabled children

DOI:

Thiopurine S-methyltransferase genetic polymorphism in the Tunisian population

DOI:

Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population

DOI:

Endurance exercises versus treadmill training in improving muscle strength and functional activities in hemiparetic cerebral palsy

DOI:

Molecular detection of circulating thyroid specific transcripts (TSHR/Tg-mRNAs) in thyroid cancer patients: Their diagnostic significance

DOI:

Salivary PCR detection of Helicobacter pylori DNA in Egyptian patients with dyspepsia

DOI:

Goldenhar syndrome with skin tags on the chest wall

DOI:

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