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Search Results - Al-Azkawi , Hanan
Search Results - Al-Azkawi , Hanan
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Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience
by
Badi, Maryam K. Al
,
Azkawi, Hanan S. Al
,
Yahyaei, Mouza S. Al
,
Mula-Abed, Waad A
,
Senani, Aisha M. Al
Published in
Saudi medical journal
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Newborn with Dilated Cardiomyopathy Secondary to Vitamin D Deficiency
by
Al Azkawi, Hanan
,
Al Mutair, Angham
Published in
Case reports in pediatrics
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A Novel Mutation Causing 17 - β - Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature
by
Mula-Abed , Waad-Allah S
,
Nahavandi , Nahid
,
Al-Kusaibi , Ghariba
,
Al-Azkawi , Hanan
,
Al-Kindi , Manal
,
Al-Sinani , Aisha
Published in
Oman medical journal
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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency
by
Yau, Mabel
,
Haider, Shozeb
,
Khattab, Ahmed
,
Ling, Chen
,
Mathew, Mehr
,
Zaidi, Samir
,
Bloch, Madison
,
Patel, Monica
,
Ewert, Sinead
,
Abdullah, Wafa
,
Toygar, Aysenur
,
Mudryi, Vitalii
,
Badi, Maryam Al
,
Alzubdi, Mouch
,
Wilson, Robert C.
,
Azkawi, Hanan Said Al
,
Ozdemir, Hatice Nur
,
Abu-Amer, Wahid
,
Hertecant, Jozef
,
Razzaghy-Azar, Maryam
,
Funder, John W.
,
Senani, Aisha Al
,
Sun, Li
,
Kim, Se-Min
,
Yuen, Tony
,
Zaidi, Mone
,
New, Maria I.
Published in
Proceedings of the National Academy of Sciences - PNAS
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A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred
by
Yau, Mabel
,
Azkawi, Hanan Said Al
,
Haider, Shozeb
,
Khattab, Ahmed
,
Badi, Maryam Al
,
Abdullah, Wafa
,
Senani, Aisha Al
,
Wilson, Robert C.
,
Yuen, Tony
,
Zaidi, Mone
,
New, Maria I.
Published in
Annals of the New York Academy of Sciences
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Hormonal, anthropometric and lipid factors associated with idiopathic pubertal gynecomastia
by
Al Alwan, Ibrahim
,
Al Azkawi, Hanan
,
Badri, Motasim
,
Tamim, Hani
,
Al Dubayee, Mohammed
,
Tamimi, Waleed
Published in
Annals of Saudi medicine
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Two Siblings with Familial Chylomicronemia Syndrome: Disease Course and Effectiveness of Early Treatment
by
al-Azkawi, Hanan
,
AlAlwan, Ibrahim
Published in
Case Reports in Medicine
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Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy
by
Al-Badi, Maryam K
,
Al-Azkawi, Hanan S
,
Al-Yahyaei, Mouza S
,
Mula-Abed, Waad A
,
Al-Senani, Aisha M
Published in
Saudi medical journal
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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11ß- hydroxysteroid dehydrogenase type 2 deficiency
by
Yau, Mabel
,
Haider, Shozeb
,
Khattab, Ahmed
,
Ling, Chen
,
Mathew, Mehr
,
Zaidi, Samir
,
Bloch, Madison
,
Patel, Monica
,
Ewert, Sinead
,
Abdullah, Wafa
,
Toygar, Aysenur
,
Mudryi, Vitalii
,
Badi, Maryam Al
,
Alzubdi, Mouch
,
Wilson, Robert C
,
Al Azkawi, Hanan Said
,
Ozdemir, Hatice Nur
,
Abu-Amer, Wahid
,
Hertecant, Jozef
,
Razzaghy-Azar, Maryam
,
Funder, John W
,
Al Senani, Aisha
,
Sun, Li
,
Kim, Se-Min
,
Yuen, Tony
,
Zaidi, Mone
,
New, Maria I
Published in
Proceedings of the National Academy of Sciences - PNAS
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Two siblings with familial chylomicronemia syndrome: disease course and effectiveness of early treatment
by
Al Azkawi, Hanan
,
Alalwan, Ibrahim
Published in
Case reports in medicine
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A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature
by
Al-Sinani, Aisha
,
Mula-Abed, Waad-Allah S
,
Al-Kindi, Manal
,
Al-Kusaibi, Ghariba
,
Al-Azkawi, Hanan
,
Nahavandi, Nahid
Published in
Oman medical journal
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