Miroslav Zivicnjak
Overview
Explore the profile of Miroslav Zivicnjak including associated specialties, affiliations and a list of published articles.
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Articles
28
Citations
327
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Recent Articles
1.
Bokenkamp A, Bouts A, van der Weerd N, Levtchenko E, Haffner D, Zivicnjak M
Pediatr Nephrol
. 2024 Sep;
40(3):701-703.
PMID: 39292251
Schimke immuno-osseous-dysplasia (SIOD) is an autosomal recessive systemic disease due to pathogenic variants in SMARCAL1. Manifestations include nephrotic syndrome (NS), kidney failure, T-cell dysfunction, vaso-occlusive disease, and disproportionate short stature,...
2.
Lahring J, Leifheit-Nestler M, Ewert A, Herzig N, Koppl C, Pott V, et al.
J Clin Endocrinol Metab
. 2024 Jul;
110(2):e218-e230.
PMID: 39049782
Context: The pathophysiology of cystinosis-associated metabolic bone disease is complex. Objective: We hypothesized a disturbed interaction between osteoblasts and osteoclasts. Methods: This binational cross-sectional multicenter study included 103 patients with...
3.
Brugelmann M, Muller S, Bohlen A, Hohenfellner K, Buscher A, Kemper M, et al.
Pediatr Nephrol
. 2024 Jun;
39(10):3067-3077.
PMID: 38850407
Background: Infantile nephropathic cystinosis (INC) is a rare lysosomal storage disorder, mostly and often firstly affecting the kidneys, together with impaired disharmonious growth and rickets, eventually resulting in progressive chronic...
4.
Muller S, Kluck R, Jagodzinski C, Brugelmann M, Hohenfellner K, Buscher A, et al.
Pediatr Nephrol
. 2023 Jul;
38(12):3989-3999.
PMID: 37415042
Background: Infantile nephropathic cystinosis (INC) is a systemic lysosomal storage disease causing intracellular cystine accumulation, resulting in renal Fanconi syndrome, progressive kidney disease (CKD), rickets, malnutrition, and myopathy. An INC-specific...
5.
Ewert A, Rehberg M, Schlingmann K, Hiort O, John-Kroegel U, Metzing O, et al.
J Clin Endocrinol Metab
. 2023 Apr;
108(10):e998-e1006.
PMID: 37097907
Context: Burosumab has been approved for the treatment of children and adults with X-linked hypophosphatemia (XLH). Real-world data and evidence for its efficacy in adolescents are lacking. Objective: To assess...
6.
Maier S, Zivicnjak M, Grigull L, Hennermann J, Aries C, Maecker-Kolhoff B, et al.
JIMD Rep
. 2022 Jul;
63(4):371-378.
PMID: 35822096
Mucopolysaccharidosis type I (MPS I) is an autosomal-recessive metabolic disorder caused by an enzyme deficiency of lysosomal alpha-l-iduronidase (IDUA). Haematopoietic stem cell transplantation (HSCT) is the therapeutic option of choice...
7.
Kluck R, Muller S, Jagodzinski C, Hohenfellner K, Buscher A, Kemper M, et al.
J Inherit Metab Dis
. 2022 Jan;
45(2):192-202.
PMID: 34989402
Children with infantile nephropathic cystinosis (INC), an inherited lysosomal storage disease resulting in cystine accumulation in all body cells, are prone to progressive chronic kidney disease (CKD), impaired growth and...
8.
Jagodzinski C, Mueller S, Kluck R, Froede K, Pavicic L, Gellermann J, et al.
Pediatr Nephrol
. 2021 Sep;
37(4):859-869.
PMID: 34542703
Background: Recombinant human growth hormone (rhGH) is frequently used for treatment of short stature in children with chronic kidney disease (CKD) prior to kidney transplantation (KT). To what extent this...
9.
Grohs J, Rebling R, Froede K, Hmeidi K, Pavicic L, Gellermann J, et al.
Pediatr Nephrol
. 2021 Feb;
36(7):1871-1880.
PMID: 33620573
Background: Short stature is a frequent complication after pediatric kidney transplantation (KT). Whether the type of transplantation and prior treatment with recombinant human growth hormone (GH) affects post-transplant growth, is...
10.
Ewert A, Leifheit-Nestler M, Hohenfellner K, Buscher A, Kemper M, Oh J, et al.
J Clin Endocrinol Metab
. 2020 May;
105(8).
PMID: 32413117
Context: Children with nephropathic cystinosis (NC) show persistent hypophosphatemia, due to Fanconi syndrome, as well as mineral and bone disorders related to chronic kidney disease (CKD); however, systematic analyses are...