An international consensus approach to the management of atypical hemolytic uremic syndrome in children

C Loirat, F Fakhouri, G Ariceta, N Besbas, M Bitzan… - Pediatric …, 2016 - Springer
… against serogroup B which predominates in European countries, North America, Australia
and New Zealand. While a vaccine against N. meningitis B is now available in some countries …

[HTML][HTML] A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders

N Besbas, D Karpman, D Landau, C Loirat… - Kidney international, 2006 - Elsevier
The diagnostic terms hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic
purpura (TTP) are based on historical and overlapping clinical descriptions. Advances in …

Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): a concomitant disease or a feature of FMF?

…, A Turkmen, I Akpolat, M Danaci, N Besbas… - Seminars in arthritis and …, 2001 - Elsevier
Background: Familial Mediterranean Fever (FMF) is caused by mutations in the gene
encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. …

Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study

…, M Arici, A Bakkaloglu, N Besbas… - Medicine …, 2005 - scholarship.miami.edu
Adolescent Adult Aged Aged, 80 and over Amyloidosis, Familial-etiology Child Child,
Preschool Colchicine-therapeutic use Epidemiologic Methods Familial Mediterranean Fever-…

Mutation frequency of familial Mediterranean fever and evidence for a high carrier rate in the Turkish population

…, B Balcı, A Duzova, R Topaloglu, N Besbas… - European journal of …, 2001 - nature.com
… In our present study, the number of amyloidosis is low (n=16) therefore a clearcut analysis …
The results of the carrier rates in Turkish population are similar to Ashkenazi and North African …

[HTML][HTML] Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome

G Ariceta, N Besbas, S Johnson, D Karpman… - Pediatric …, 2009 - Springer
This guideline for the investigation and initial treatment of atypical hemolytic uremic syndrome
(HUS) is intended to offer an approach based on opinion, as evidence is lacking. It builds …

Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis

…, S Ozen, S Özdemir, A Bakkaloglu, N Besbas… - European journal of …, 1997 - Springer
Familial Mediterranean fever (FMF) is a genetically transmitted disease characterized by
recurrent attacks of fever and serositis. The most important complication of this disease is the …

Juvenile polyarteritis: results of a multicenter survey of 110 children

…, J Anton, N Arisoy, A Bakkaloglu, N Besbas… - The Journal of …, 2004 - Elsevier
… A questionnaire was sent to pediatric rheumatologists in centers in Europe, South America,
and North America. Patients diagnosed with PAN who were followed within the last 5 years …

[PDF][PDF] Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever

A Duzova, A Bakkaloglu, N Besbas… - Clinical and …, 2003 - academia.edu
Objectives 1) To compare the sensitivity of serum amyloid A protein (A-SAA) and other
acute phase proteins (APPs) in determining subclinical inflammation in patients with familial …

DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN

…, S Ozen, R Topaloglu, N Besbas… - Journal of the …, 2013 - journals.lww.com
… (nA/pF at −100 mV, mean ± SD, n=20) measured in HEK293T cells transfected with
empty expression … Mean ± SD (n=20) of peak inward current density from F. *P<0.05; ***P<0.001. …