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内部出版物
CNKI学位论文(4)
知网期刊论文(1)
在“
Elsevier电子期刊
”中,
命中:
4
条,耗时:小于0.01 秒
在所有数据库中总计命中:
5
条
1.
Transferrin isoelectric focusing and plasma lysosomal enzyme activities in the diagnosis and follow©\up of hereditary fructose intolerance
作者:
Marina Moraitou
;
Evangelia Dimitriou
;
Irene Mavridou
;
Helen Michelakakis
;
Helen Georgouli
;
Rafal Ploski
;
Agnieszka
Pollak
刊名:Clinica Chimica Acta
出版年:2012
2.
Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss
作者:
Mał
;
gorzata Rydzanicz
;
Maciej Wró
;
bel
;
Agnieszka
Pollak
;
Wojciec Gawę
;
cki
;
Damian Brauze
;
Magdalena Kostrzewska-Poczekaj
;
Irena Wojsyk-Banaszak
;
Urszula Lechowicz
;
Mał
;
gorzata Muell
关键词:
Non-syndromic hearing loss
;
Aminoglycoside-induced hearing loss
;
Mitochondrial DNA
;
12S rRNA
gene mutations
刊名:Biochemical and Biophysical Research Communications
出版年:2010
3.
Novel keratin 14 hotspot mutation in Dowling-Meara type of epidermolysis bullosa simplex: Strategy to avoid KRT14 pseudogene amplification by a simple approach
作者:
Monika Oł
;
dak
;
Cezary Kowalewski
;
Radosł
;
aw B. Maksym
;
Katarzyna Woź
;
niak
;
Agnieszka
Pollak
;
Marta Podgó
;
rska
;
Artur Wnorowski
;
Joanna Kosiń
;
ska
;
Rafał
;
Pł
;
oski
刊名:Journal of Dermatological Science
出版年:2010
4.
Aldolase B mutations and prevalence of hereditary fructose intolerance in a Polish population
作者:
Jakub Gruchota
;
Ewa Pronicka
;
Lech Korniszewski
;
Bartosz Stolarski
;
Agnieszka
Pollak
;
Mał
;
gorzata Rogaszewska and Rafał
;
Pł
;
oski
关键词:
ALDOB
;
Mutations
;
Hereditary fructose intolerance
;
Poland
;
Disease prevalence
刊名:Molecular Genetics and Metabolism
出版年:2006
1
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