User profiles for "author:Mahdi Salih"

Mahdi Salih

Erasmus MC
Verified email at erasmusmc.nl
Cited by 1204

Urinary extracellular vesicles and the kidney: biomarkers and beyond

M Salih, R Zietse, EJ Hoorn - American Journal of …, 2014 - journals.physiology.org
Extracellular vesicles have been isolated in various body fluids, including urine. The cargo
of urinary extracellular vesicles (uEVs) is composed of proteins and nucleic acids reflecting …

[PDF][PDF] Thyrotoxic periodic paralysis: an unusual presentation of hyperthyroidism

M Salih, CMJ Van Kinschot, RP Peeters… - Neth J Med, 2017 - njmonline.nl
Thyrotoxic periodic paralysis (TPP) is a complication of hyperthyroidism among Asians,
characterised by sudden onset of hypokalaemia and muscle paralysis. Several factors may …

Effect of lanreotide on kidney function in patients with autosomal dominant polycystic kidney disease: the DIPAK 1 randomized clinical trial

E Meijer, FW Visser, RMM Van Aerts, CJ Blijdorp… - Jama, 2018 - jamanetwork.com
Importance Autosomal dominant polycystic kidney disease (ADPKD) is characterized by
progressive cyst formation in both kidneys and loss of renal function, eventually leading to a …

The phosphorylated sodium chloride cotransporter in urinary exosomes is superior to prostasin as a marker for aldosteronism

N van der Lubbe, PM Jansen, M Salih, RA Fenton… - …, 2012 - Am Heart Assoc
Urinary exosomes are vesicles derived from renal tubular epithelial cells. Exosomes often
contain several disease-associated proteins and are thus useful targets for identifying …

[HTML][HTML] Update on controls for isolation and quantification methodology of extracellular vesicles derived from adipose tissue mesenchymal stem cells

M Franquesa, MJ Hoogduijn, E Ripoll, F Luk… - Frontiers in …, 2014 - frontiersin.org
The research field on extracellular vesicles (EV) has rapidly expanded in recent years due to
the therapeutic potential of EV. Adipose tissue human mesenchymal stem cells (ASC) may …

A missense mutation in the extracellular domain of αENaC causes Liddle syndrome

M Salih, I Gautschi, MX Van Bemmelen… - Journal of the …, 2017 - journals.lww.com
Liddle syndrome is an autosomal dominant form of hypokalemic hypertension due to
mutations in the β-or γ-subunit of the epithelial sodium channel (ENaC). Here, we describe a …

Proteomics of urinary vesicles links plakins and complement to polycystic kidney disease

M Salih, JA Demmers, K Bezstarosti… - Journal of the …, 2016 - journals.lww.com
Novel therapies in autosomal dominant polycystic kidney disease (ADPKD) signal the need
for markers of disease progression or response to therapy. This study aimed to identify …

Rationale and design of the DIPAK 1 study: a randomized controlled clinical trial assessing the efficacy of lanreotide to Halt disease progression in autosomal …

E Meijer, JPH Drenth, H d'Agnolo, NF Casteleijn… - American Journal of …, 2014 - Elsevier
Background There are limited therapeutic options to slow the progression of autosomal
dominant polycystic kidney disease (ADPKD). Recent clinical studies indicate that …

Urinary extracellular vesicles as markers to assess kidney sodium transport

M Salih, RA Fenton, R Zietse… - Current Opinion in …, 2016 - journals.lww.com
Urinary extracellular vesicles as markers to assess kidney s... : Current Opinion in Nephrology
and Hypertension Urinary extracellular vesicles as markers to assess kidney sodium transport …

Lanreotide reduces liver growth in patients with autosomal dominant polycystic liver and kidney disease

RMM van Aerts, W Kievit, HMA D'Agnolo, CJ Blijdorp… - Gastroenterology, 2019 - Elsevier
Background & Aims Polycystic liver disease is the most common extrarenal manifestation of
autosomal dominant polycystic kidney disease (ADPKD). There is need for robust long-term …