Hazem S Awad
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Explore the profile of Hazem S Awad including associated specialties, affiliations and a list of published articles.
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9
Citations
122
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0
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Recent Articles
1.
Borzych-Duzalka D, Shroff R, Ranchin B, Zhai Y, Paglialonga F, Kari J, et al.
Kidney Int Rep
. 2024 Jun;
9(6):1694-1704.
PMID: 38899176
Introduction: Fluid and salt overload in patients on dialysis result in high blood pressure (BP), left ventricular hypertrophy (LVH) and hemodynamic instability, resulting in cardiovascular morbidity. Methods: Analysis of 910...
2.
Deutsch K, Klambt V, Kitzler T, Jobst-Schwan T, Schneider R, Buerger F, et al.
Genes Dis
. 2024 Jun;
11(5):101111.
PMID: 38868576
No abstract available.
3.
Habeeb S, Yamin H, Simkova E, Awad H, Alhammadi E, Eid L, et al.
Pediatr Nephrol
. 2022 Nov;
38(5):1687-1692.
PMID: 36352270
Background: Peritonitis is an important complication and cause of morbidity in patients undergoing peritoneal dialysis (PD). Corynebacterium species, often considered skin and mucosal contaminants, are a rare cause of PD-associated...
4.
Wu C, Lim T, Wang C, Seltzsam S, Zheng B, Schierbaum L, et al.
Eur Urol Open Sci
. 2022 Oct;
44:106-112.
PMID: 36185583
Background: Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease among children and adults younger than 30 yr. In our previous...
5.
Wang C, Seltzsam S, Zheng B, Wu C, Nicolas-Frank C, Yousef K, et al.
Am J Med Genet A
. 2022 Jan;
188(5):1355-1367.
PMID: 35040250
Spina bifida (SB) is the second most common nonlethal congenital malformation. The existence of monogenic SB mouse models and human monogenic syndromes with SB features indicate that human SB may...
6.
Seltzsam S, Wang C, Zheng B, Mann N, Connaughton D, Wu C, et al.
Genet Med
. 2021 Dec;
24(2):307-318.
PMID: 34906515
Purpose: Congenital anomalies of the kidneys and urinary tract (CAKUT) constitute the leading cause of chronic kidney disease in children. In total, 174 monogenic causes of isolated or syndromic CAKUT...
7.
Zheng B, Wang C, Seltzsam S, Schneider S, Schierbaum L, Wu W, et al.
Am J Med Genet A
. 2021 Sep;
188(1):310-313.
PMID: 34525250
Congenital anomalies of the kidneys and urinary tract (CAKUT) constitute the most common cause of early-onset chronic kidney disease. In a previous study, we identified a heterozygous truncating variant in...
8.
Al Romaili D, Al-Hussain T, Awad H, Saadeh S, Al-Hassoun I, Al-Shareef T
Int J Pediatr Adolesc Med
. 2020 Jan;
6(4):146-150.
PMID: 31890840
Background: Idiopathic nephrotic syndrome (INS) is a common pediatric disease. Minimal change disease (MCD) is the most common histopathological subtype and usually has good prognosis. However, in less common presentations,...
9.
van der Ven A, Connaughton D, Ityel H, Mann N, Nakayama M, Chen J, et al.
J Am Soc Nephrol
. 2018 Aug;
29(9):2348-2361.
PMID: 30143558
Background: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most prevalent cause of kidney disease in the first three decades of life. Previous gene panel studies showed...