Vol. 13 No. 1 (2012) | Egyptian Journal of Medical Human Genetics

Role of Gal and GalNAc containing glycans in various physiological processes

MRM Hussain, M Hassan, I Afzal, A Afzal

1-9

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Genetics of obesity

RM Shawky, DI Sadik

11-17

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Molecular analysis of MECP2 gene in Egyptian patients with Rett syndrome

MS Zaki, WE Sharaf El-Din, GM Hamdy, IH Kamal, AK Abdel Aleem

19-27

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Phototherapy and DNA changes in full term neonates with hyperbilirubinemia

MYZ El-Abdin, MA El-Salam, MY Ibrhim, SSM Koraa, E Mahmoud

29-35

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Role of treadmill training versus suspension therapy on balance in children with Down syndrome

GH El-Meniawy, HM Kamal, SA Elshemy

37-43

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Profile of genetic disorders prevalent in northeast region of Cairo, Egypt

RM Shawky, NS Elsayed, DS Ibrahim, NS Seifeldin

45-62

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Modulation of back geometry in children with spastic diplegic cerebral palsy via hippotherapy training

GH El-Meniawy, NS Thabet

63-71

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Serum amino acid abnormalities in pediatric patients with chronic renal failure with and without history of thromboembolic manifestations

MA El Sawy, MM Zaki, IZ EL-Hakim, ME Mowafy, HS Al-Abd

73-80

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Role of ascitic fluid C3 in spontaneous bacterial peritonitis

AT Kamal, EN Osman, RY Shahin

81-85

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Pilot study for assessment of prevalence of intrafamilial hepatitis C transmission in relation to salivary viral load among infected patients with and without chronic renal failure

H El Tayeb, NA El Nakeeb, MM Sayed, WA Yousry, SHA Agwa

87-92

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Haemophilia A patients are not at increased risk of hepatitis A virus infection: An Egyptian experience

AAG Tantawy, EAM Algohary, SMA El-Ghany, SF Elhadary

93-97

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Hospital-acquired pneumonia in critically ill children: Incidence, risk factors, outcome and diagnosis with insight on the novel diagnostic technique of multiplex polymerase chain reaction

MGE Mansour, S Bendary

99-105

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Case Report: Multiple pterygium syndrome with marked pterygia of the fingers and MRI changes in the spine

RM Shawky, S Elsayed, N Gaboon

107-113

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Case Report: Trigonocephaly and Dandy walker variant in an Egyptian child – Probable mild Opitz trigonocephaly C syndrome

RM Shawky, HS Abd-Elkhalek

115-118

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Educational Corner

MSZ Salem

119-125

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 13 No. 1 (2012) / Articles

Articles

Role of Gal and GalNAc containing glycans in various physiological processes

Genetics of obesity

Molecular analysis of MECP2 gene in Egyptian patients with Rett syndrome

Phototherapy and DNA changes in full term neonates with hyperbilirubinemia

Role of treadmill training versus suspension therapy on balance in children with Down syndrome

Profile of genetic disorders prevalent in northeast region of Cairo, Egypt

Modulation of back geometry in children with spastic diplegic cerebral palsy via hippotherapy training

Serum amino acid abnormalities in pediatric patients with chronic renal failure with and without history of thromboembolic manifestations

Role of ascitic fluid C3 in spontaneous bacterial peritonitis

Pilot study for assessment of prevalence of intrafamilial hepatitis C transmission in relation to salivary viral load among infected patients with and without chronic renal failure

Haemophilia A patients are not at increased risk of hepatitis A virus infection: An Egyptian experience

Hospital-acquired pneumonia in critically ill children: Incidence, risk factors, outcome and diagnosis with insight on the novel diagnostic technique of multiplex polymerase chain reaction

Case Report: Multiple pterygium syndrome with marked pterygia of the fingers and MRI changes in the spine

Case Report: Trigonocephaly and Dandy walker variant in an Egyptian child – Probable mild Opitz trigonocephaly C syndrome

Educational Corner

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