about
Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patientsEpidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4.Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment.Surgical management of renovascular hypertension in children and young adults: a 13-year experienceAn immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissuesRenal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic SyndromeGenetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group
P50
Q36241014-4F7B27A6-996B-4F0A-B238-9050D7A67F28Q48357912-68D079FF-687D-4022-BA7E-11A60A10A4CCQ48366696-F7E4B5CC-83DC-42BF-AB69-F5234E4BEBD0Q90941402-CEDDE713-1701-41D8-B134-8B4196D2BFFAQ91276869-BA443F7A-4B25-4DA3-8650-45853B8EF7A2Q94677862-BED5F44D-C023-4474-9053-A05B5060AE42Q95936586-C8C9CCA5-C8BA-4056-8254-672CFAFAF49F
P50
description
researcher ORCID ID = 0000-0003-1194-0164
@en
wetenschapper
@nl
name
Fatih Ozaltin
@ast
Fatih Ozaltin
@en
Fatih Ozaltin
@es
Fatih Ozaltin
@nl
type
label
Fatih Ozaltin
@ast
Fatih Ozaltin
@en
Fatih Ozaltin
@es
Fatih Ozaltin
@nl
prefLabel
Fatih Ozaltin
@ast
Fatih Ozaltin
@en
Fatih Ozaltin
@es
Fatih Ozaltin
@nl
P31
P496
0000-0003-1194-0164