Jasmina Comic
Overview
Explore the profile of Jasmina Comic including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
7
Citations
17
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Riedhammer K, Simmendinger H, Tasic V, Putnik J, Abazi-Emini N, Stajic N, et al.
Clin Genet
. 2024 Jan;
105(4):406-414.
PMID: 38214412
Alport syndrome (AS) shows a broad phenotypic spectrum ranging from isolated microscopic hematuria (MH) to end-stage kidney disease (ESKD). Monoallelic disease-causing variants in COL4A3/COL4A4 have been associated with autosomal dominant...
2.
Riedhammer K, Nguyen T, Kosukcu C, Calzada-Wack J, Li Y, Assia Batzir N, et al.
Kidney Int
. 2023 Dec;
105(4):844-864.
PMID: 38154558
Congenital anomalies of the kidney and urinary tract (CAKUT) are the predominant cause for chronic kidney disease below age 30 years. Many monogenic forms have been discovered due to comprehensive...
3.
Implication of dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Riedhammer K, Nguyen T, Kosukcu C, Calzada-Wack J, Li Y, Saygili S, et al.
medRxiv
. 2023 Mar;
PMID: 36993625
Background: Congenital anomalies of the kidney and urinary tract (CAKUT) are the predominant cause for chronic kidney disease below 30 years of age. Many monogenic forms have been discovered mainly...
4.
Riedhammer K, Comic J, Tasic V, Putnik J, Abazi-Emini N, Paripovic A, et al.
Eur J Hum Genet
. 2023 Mar;
31(6):674-680.
PMID: 36922632
Individuals with congenital anomalies of the kidney and urinary tract (CAKUT) show a broad spectrum of malformations. CAKUT can occur in an isolated fashion or as part of a syndromic...
5.
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age
Gunthner R, Knipping L, Jeruschke S, Satanoskij R, Lorenz-Depiereux B, Hemmer C, et al.
Front Med (Lausanne)
. 2022 Nov;
9:953643.
PMID: 36341250
X-linked Alport syndrome (AS) caused by hemizygous disease-causing variants in primarily affects males. Females with a heterozygous state show a diverse phenotypic spectrum ranging from microscopic hematuria to end-stage kidney...
6.
Najafi M, Riedhammer K, Rad A, Najarzadeh Torbati P, Berutti R, Schule I, et al.
Front Pediatr
. 2022 Oct;
10:974840.
PMID: 36245711
Background: Steroid resistant nephrotic syndrome (SRNS) represents a significant renal disease burden in childhood and adolescence. In contrast to steroid sensitive nephrotic syndrome (SSNS), renal outcomes are significantly poorer in...
7.
Comic J, Riedhammer K, Gunthner R, Schaaf C, Richthammer P, Simmendinger H, et al.
Front Med (Lausanne)
. 2022 Sep;
9:957733.
PMID: 36117978
Disease-causing variants in 5 are associated with type-IV-collagen-related nephropathy, a genetically and phenotypically multifaceted disorder comprising Alport syndrome (AS) and thin basement membrane nephropathy (TBMN) and autosomal, X-linked and a...