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Al-Haggar, Mohammad
54  Ergebnisse:
Personensuche X
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1

Biallelic Variants in MNS1 Are Associated with Laterality D..:

Hjeij, Rim ; Leslie, Joseph ; Rizk, Hoda...
Cells.  13 (2024)  12 - p. 1017 , 2024
Link: https://doi.org/10.3390/..
 
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2

Analysis of the association of NPHS2 and ACTN4 genes polymo..:

al-azzawy, Mohammed F. ; Al-Haggar, Mohammad ; ElSaid, Afaf M..
Molecular Biology Reports.  50 (2023)  5 - p. 4481-4490 , 2023
Link: https://doi.org/10.1007/..
 
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3

Recurrence pattern of non-syndromic familial congenital hea..:

Rakha, Shaimaa ; Mohy-Eldeen, Rehab ; Al-Haggar, Mohammad.
BMC Pediatrics.  22 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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4

MRI CSF flowmetry in evaluation of different neurological d..:

Ahmad, Nermin ; Salama, Dina ; Al-Haggar, Mohammad
Egyptian Journal of Radiology and Nuclear Medicine.  52 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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5

Novel homozygousSLC29A3mutations among two unrelated Egypti..:

Al-Haggar, Mohammad ; Salem, Nanees ; Wahba, Yahya...
Pediatric Diabetes.  16 (2014)  4 - p. 305-316 , 2014
Link: https://doi.org/10.1111/..
 
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6

Partial expression of ornithine transcarbamylase deficiency..:

Al-Haggar, Mohammad ; Largiadèr, Carlo R. ; Abdel-Hady, Dina...
International Journal of Gynecology & Obstetrics.  124 (2013)  2 - p. 174-175 , 2013
Link: https://doi.org/10.1016/..
 
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7

Sporadic Fibrodysplasia Ossificans Progressiva in an Egypti..:

Al-Haggar, Mohammad ; Ahmad, Nermin ; Yahia, Sohier...
Case Reports in Genetics.  2013 (2013)  - p. 1-8 , 2013
Link: https://doi.org/10.1155/..
 
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8

Ultrastructural skin changes in Egyptian mandibuloacral dys..:

Al-Haggar, Mohammad ; Shams, Amany ; Madej-Pilarczyk, Agnieszka..
Journal of Clinical Pathology.  66 (2013)  11 - p. 1000-1004 , 2013
Link: https://doi.org/10.1136/..
 
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9

Mutation analysis of the GLUT2 gene in three unrelated Egyp..:

Al-Haggar, Mohammad ; Sakamoto, Osamu ; Shaltout, Ali...
Clinical and Experimental Nephrology.  16 (2012)  4 - p. 604-610 , 2012
Link: https://doi.org/10.1007/..
 
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10

Fanconi Bickel Syndrome: Novel Mutations inGLUT 2Gene Causi..:

Al-Haggar, Mohammad ; Sakamoto, Osamu ; Shaltout, Ali...
Case Reports in Nephrology.  2011 (2011)  - p. 1-5 , 2011
Link: https://doi.org/10.1155/..
 
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11

p.R672C Mutation of MYH3 Gene in an Egyptian Infant Present..:

Al-Haggar, Mohammad ; Yahia, Soheir ; Damjanovich, Kristy...
The Indian Journal of Pediatrics.  78 (2010)  1 - p. 103-105 , 2010
Link: https://doi.org/10.1007/..
 
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12

Familial hypomagnesemia with hypercalciuria and nephrocalci..:

Al-Haggar, Mohammad ; Bakr, Ashraf ; Tajima, Toshihiro...
Clinical and Experimental Nephrology.  13 (2009)  4 - p. 288-294 , 2009
Link: https://doi.org/10.1007/..
 
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13

Vitamin E and N-Acetylcysteine as Antioxidant Adjuvant Ther..:

Al-Tonbary, Youssef ; Al-Haggar, Mohammad ; EL-Ashry, Rasha...
Advances in Hematology.  2009 (2009)  - p. 1-5 , 2009
Link: https://doi.org/10.1155/..
 
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14

Correlation of thyroid and growth hormones to chromosomal i..:

Al-Haggar, Mohammad ; Al-Morsy, Zakaria ; Yahia, Sohier...
The Indian Journal of Pediatrics.  75 (2008)  7 - p. 679-684 , 2008
Link: https://doi.org/10.1007/..
 
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15

Impact of long-term oral iron supplementation in breast-fed..:

Abdelrazik, Nabil ; Al-Haggar, Mohammad ; Al-Marsafawy, Hala...
The Indian Journal of Pediatrics.  74 (2007)  8 - p. 739-745 , 2007
Link: https://doi.org/10.1007/..
 
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