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Irina Golovleva

Kontaktinformation
Befattning:	Universitetslektor, adjungerad
Verksam vid:	Medicinsk biovetenskap
Avdelning:	Medicinsk och klinisk genetik
Adress:	Umeå universitet SE-901 85 Umeå Sverige
Besöksadress:	By 6M, vån 1, Sjukhusområdet
Tel:	+46 90 785 68 20
Fax:	+46 90 785 44 84
E-postadress:	irina.golovleva@medbio.umu.se E-post
Webbsida:	http://www.medbio.umu.se/om-institutionen/personal/golovleva-irina/ Webbsida

Publikationer

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Författare	Titel	År	Fulltext
Safavi, S. Forestier, Erik Golovleva, Irina; et al.	Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia Leukemia, 27(1): 248-250	2013	-
Reinis, Ainars Golovleva, Irina Köhn, Linda; et al.	Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation Acta Ophthalmologica, 91(3): 259-266	2013	-
Jahns, Anika C Golovleva, Irina Palmer, Ruth H; et al.	Spatial distribution of bacterial-fungal communities in facial skin. Journal of dermatological science (Amsterdam), 70(1): 71-73	2013	-
Andersson, Charlotta Li, Xingru Lorenz, Fryderyk; et al.	Reduction in WT1 Gene Expression During Early Treatment Predicts the Outcome in Patients With Acute Myeloid Leukemia Diagnostic molecular pathology (Print), 21(4): 225-233	2012	-
Alexeyev, Oleg A Lundskog, Bertil Ganceviciene, Ruta; et al.	Pattern of tissue invasion by Propionibacterium acnes in acne vulgaris Journal of dermatological science (Amsterdam), 67(1): 63-66	2012	-
Zachariadis, V Gauffin, F Kuchinskaya, E; et al.	The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial Leukemia	2011	-
Andersen, Mette K. Autio, Kirsi Barbany, Gisela; et al.	Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols British Journal of Haematology, 155(2): 235-243	2011	-
Lindstrand, Anna Malmgren, Helena Verri, Annapia; et al.	Molecular and clinical characterization of patients with overlapping 10p deletions American Journal of Medical Genetics. Part A, 152A(5): 1233-1243	2010	-
Köhn, Linda Kohl, Susanne Bowne, Sara J; et al.	PITPNM3 is an uncommon cause of cone and cone-rod dystrophies. Ophthalmic Genetics, 31(3): 139-140	2010	-
Burstedt, Marie Golovleva, Irina	Central Retinal Findings in Bothnia Dystrophy Caused by RLBP1 Sequence Variation Archives of ophthalmology (1960), 128(8): 989-995	2010	-

Sidansvarig: Åsa Lundsten
2010-11-02