Martin Pohl
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Explore the profile of Martin Pohl including associated specialties, affiliations and a list of published articles.
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81
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1506
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Recent Articles
1.
Barbour S, Coppo R, Er L, Pillebout E, Russo M, Alpers C, et al.
Clin J Am Soc Nephrol
. 2024 Jan;
19(4):438-451.
PMID: 38261310
Background: Nephritis is a common manifestation of IgA vasculitis and is morphologically indistinguishable from IgA nephropathy. While MEST-C scores are predictive of kidney outcomes in IgA nephropathy, their value in...
2.
Moritz L, Schumann A, Pohl M, Kottgen A, Hannibal L, Spiekerkoetter U
Clin Biochem
. 2023 Dec;
123:110703.
PMID: 38097032
Chronic kidney disease (CKD) affects over 0.5 billion people worldwide across their lifetimes. Despite a growingly ageing world population, an increase in all-age prevalence of kidney disease persists. Adult-onset forms...
3.
Schmitz J, Kracht J, Evert K, Wenzel J, Schemmerer M, Lehmann U, et al.
Am J Transplant
. 2023 Dec;
24(3):491-497.
PMID: 38072120
Immunocompromised patients are at risk of chronic hepatitis E (HEV) infection. Recurrent T cell and borderline rejections in a pediatric patient with high HEV copy numbers led us to study...
4.
Ujkic L, Haeffner K, Praus F, Pohl M, Pohlmann P, Kroenig M, et al.
Eur Urol Open Sci
. 2023 Nov;
57:106-112.
PMID: 38020523
Background: Duplex kidneys may be associated with additional pathologies with an indication for surgery. Various surgical approaches have been described. However, little is known about long-term outcomes and quality of...
5.
Prytula A, Shroff R, Krupka K, Deschepper E, Bacchetta J, Ariceta G, et al.
Kidney Int Rep
. 2023 Jan;
8(1):81-90.
PMID: 36644359
Introduction: Little is known about the consequences of deranged chronic kidney disease-mineral and bone disorder (CKD-MBD) parameters on kidney allograft function in children. We examined a relationship between these parameters...
6.
Fischerova S, Pohl M
Cas Lek Cesk
. 2022 Nov;
161(5):212-219.
PMID: 36443102
The so-called Hippocratic Oath is based on a standardized form of oath in the ancient world and is undoubtedly the most famous, most discussed and most commented part of the...
7.
Butzer S, Hennies I, Gimpel C, Gellermann J, Schalk G, Konig S, et al.
BMC Pediatr
. 2022 Oct;
22(1):570.
PMID: 36195856
Background: IgA vasculitis (IgAV) is the most common form of systemic vasculitis in childhood and frequently involves the kidney. A minority of patients with IgA vasculitis nephritis (IgAVN), especially those...
8.
Konig J, Karsay R, Gerss J, Schlingmann K, Dahmer-Heath M, Telgmann A, et al.
Kidney Int Rep
. 2022 Sep;
7(9):2016-2028.
PMID: 36090483
Introduction: Nephronophthisis (NPH) comprises a group of rare disorders accounting for up to 10% of end-stage kidney disease (ESKD) in children. Prediction of kidney prognosis poses a major challenge. We...
9.
Trefzer L, Schwieger-Briel A, Nystrom A, Conradt G, Pohl M, Miernik A, et al.
JAMA Dermatol
. 2022 Aug;
158(9):1057-1062.
PMID: 35921091
Importance: Kidney-urinary tract (KUT) manifestations cause substantial morbidity in patients with junctional epidermolysis bullosa (JEB), but the spectrum of disease severity and the clinical course have been poorly characterized. Objective:...
10.
Niessl C, Boulesteix A, Oh J, Palm K, Schlingmann P, Wygoda S, et al.
Mol Genet Metab
. 2022 Jul;
136(4):268-273.
PMID: 35835062
Infantile nephropathic cystinosis, due to impaired transport of cystine out of lysosomes, occurs with an incidence of 1 in 100-200,000 live births. It is characterized by renal Fanconi syndrome in...