E-LIB Suche - Ergebnisse für: AL Azkawi, Hanan

1

Newborn with Dilated Cardiomyopathy Secondary to Vitamin D ..:

Al Azkawi, Hanan ; Al Mutair, Angham
Case Reports in Pediatrics. 2012 (2012) - p. 1-5 , 2012

Link: https://doi.org/10.1155/..

2

Two Siblings with Familial Chylomicronemia Syndrome: Diseas..:

AL Azkawi, Hanan ; AlAlwan, Ibrahim
Case Reports in Medicine. 2010 (2010) - p. 1-5 , 2010

Link: https://doi.org/10.1155/..

3

Clinical, genetic, and structural basis of apparent mineral..:

Yau, Mabel ; Haider, Shozeb ; Khattab, Ahmed...
Proceedings of the National Academy of Sciences. 114 (2017) 52 - p. , 2017

Link: https://doi.org/10.1073/..

4

Clinical, genetic, and structural basis of apparent mineral..:

Yau, Mabel ; Haider, Shozeb ; Khattab, Ahmed...
Proceedings of the National Academy of Sciences of the United States of America. 114 (2017) 52 - p. E11248-E11256 , 2017

Link: https://www.jstor.org/st..

5

A novel mutation inHSD11B2causes apparent mineralocorticoid..:

Yau, Mabel ; Azkawi, Hanan Said Al ; Haider, Shozeb...
Annals of the New York Academy of Sciences. 1376 (2016) 1 - p. 65-71 , 2016

Link: https://doi.org/10.1111/..

6

Hormonal, anthropometric and lipid factors associated with ..:

Ibrahim Al Alwan ; Hanan Al Azkawi ; Motasim Badri...
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2013.579. , 2013

Link: https://doi.org/10.5144/..

7

Newborn with Dilated Cardiomyopathy Secondary to Vitamin D ..:

Hanan Al Azkawi ; Angham Al Mutair
http://dx.doi.org/10.1155/2012/945437. , 2012

Link: https://doi.org/10.1155/..

8

Two Siblings with Familial Chylomicronemia Syndrome: Diseas..:

Hanan AL Azkawi ; Ibrahim AlAlwan
http://dx.doi.org/10.1155/2010/807434. , 2010

Link: https://doi.org/10.1155/..

9

Clinical characteristics and phenotype-genotype review of 2..:

Al-Badi, Maryam K. ; Al-Azkawi, Hanan S. ; Al-Yahyaei, Mouza S...
Saudi Medical Journal. 40 (2019) 7 - p. 669-674 , 2019

Link: https://doi.org/10.15537..

10

A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase ..:

Aisha Al-Sinani ; Waad-Allah S. Mula-Abed ; Manal Al-Kindi...
http://www.omjournal.org/fultext_PDF.aspx?DetailsID=632&type=fultext. , 2015

Link: https://doi.org/10.5001/..

11

A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase ..:

Al-Sinani, Aisha ; Mula-Abed, Waad-Allah S ; Al-Kindi, Manal...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412451/. , 2015

Link: http://www.ncbi.nlm.nih...