Наследственный ангионевротический отёк (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Наследственный ангионевротический отёк" in Russian language version.

refsWebsite

Global rank Russian rank

2^nd place

3^rd place

4^th place

6^th place

1^st place

low place

11^th place

286^th place

6^th place

9^th place

archive.org (Global: 6^th place; Russian: 9^th place)

Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK (Октябрь 2011). A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family. Allergy. 66 (10): 1384–90. doi:10.1111/j.1398-9995.2011.02658.x. PMID 21623829. S2CID 23036731.
Bafunno V, Bova M, Loffredo S, Divella C, Petraroli A, Marone G, Montinaro V, Margaglione M, Triggiani M (Март 2014). Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations. Ann Hum Genet. 78 (2): 73–82. doi:10.1111/ahg.12052. PMID 24456027.
Weiler CR, van Dellen RG (Июль 2006). Genetic test indications and interpretations in patients with hereditary angioedema. Mayo Clin Proc. 81 (7): 958–72. doi:10.4065/81.7.958. PMID 16835976.

Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK (Октябрь 2011). A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family. Allergy. 66 (10): 1384–90. doi:10.1111/j.1398-9995.2011.02658.x. PMID 21623829. S2CID 23036731.
Bafunno V, Bova M, Loffredo S, Divella C, Petraroli A, Marone G, Montinaro V, Margaglione M, Triggiani M (Март 2014). Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations. Ann Hum Genet. 78 (2): 73–82. doi:10.1111/ahg.12052. PMID 24456027.
Weiler CR, van Dellen RG (Июль 2006). Genetic test indications and interpretations in patients with hereditary angioedema. Mayo Clin Proc. 81 (7): 958–72. doi:10.4065/81.7.958. PMID 16835976.

Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK (Октябрь 2011). A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family. Allergy. 66 (10): 1384–90. doi:10.1111/j.1398-9995.2011.02658.x. PMID 21623829. S2CID 23036731.