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Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders
Researches
Researches main page of Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders
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Research Title
Research Type
Research Year
طفرة وراثية تسبق مرحلة تضاعف الحمض النووي و تؤدي اللى متلازمة غورلين-مير
Mutations in the pre-replication complex cause Meier-Gorlin syndrome
Nature Journal
Article In Journal
1432
Show
Research Title
Research Type
Research Year
ريتوكسيماب للحالات الغير مستجيبة للعلاج من المتلازمة الكلوية عند الأطفال
Rituximab for refractory cases of childhood nephrotic syndrome
Springer Pediatrics
Article In Journal
1432
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Research Title
Research Type
Research Year
علاج متلازمة مقاومة الستيرويد الكلوي لدى الأطفال
Treatment of steroid resistant nephritic syndrome in children
Saudi Journal of Kidney Diseaeses and Transplantation
Article In Journal
1431
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Research Title
Research Type
Research Year
ظهور مقاومة كلوية للستيرويدات و مرض السكري المعتمد على الأنسولين في نفس الوقت عند طفلين صغيرين
Simultaneous onset of steroid resistant nephrotic syndrome and IDDM in two young children
BMJ publishing group
Article In Journal
1431
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Research Title
Research Type
Research Year
تسعة عشر طفرة جديدة في جين NPHS1 في مجموعة مرضى المتلازمة الكلوية الخلقية من مختلف انحاء العالم
Ninteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)
Oxford University Journals
Article In Journal
1431
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Research Title
Research Type
Research Year
التغيرات النسيجية في الأطفال المصابين بالمتلازمة الكلوية الغير مستجيبة للاستيرويد في المملكة العربية السعودية
Histopathology of steroid-resistant nephritic syndrome in children living in the kingdom of Saudi Arabia
Springer Pediatrics
Article In Journal
1430
Show
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