A. Kuzmin

发表

Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population.

A. Brown, A. Goltsov, S. Woo, 1996, Pediatrics.

An immunomodulatory procedure that stabilizes transgene expression and permits readministration of E1-deleted adenovirus vectors.

R. Eisensmith, A. Kuzmin, O. Galenko, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Prospects for the treatment of phenylketonuria by gene therapy

R. Eisensmith, A. Kuzmin, V. Krougliak, 1999 .

Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans.

F. Güttler, A. Goltsov, L. Tyfield, 1995, American journal of human genetics.

[Influence of the antihypoxantic therapy on children with generalized peritonitis].

V. G. Rodionov, A. Kuzmin, E. V. Terekhova, 2016, Khirurgiia.

[Treatment of diffuse peritonitis in children].

V. G. Rodionov, Y. Frolova, A. Kuzmin, 2015, Khirurgiia.

The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg

S. Shevtsov, A. Kuzmin, E. Schwartz, 1996, Journal of Inherited Metabolic Disease.

Phenylketonuria in Costa Rica: preliminary spectrum of PAH mutations and their associations with highly polymorphic haplotypes.

R. Barrantes, A. Goltsov, S. Woo, 1996, Human heredity.

Haplotypes and mutations of the PAH locus in Egyptian families with PKU

N. Meguid, M. El-Awady, S. Temtamy, 1999, European Journal of Human Genetics.

IFN-γ sensitization of prostate cancer cells to Fas-mediated death: A gene therapy approach

M. Meseck, Shu-Hsia Chen, S. Canfield, 2003 .

[Our experience in treating children with acute destructive pancreatitis].

A. Kuzmin, A. Varlamov, V. A. Zavyalkin, 2017, Khirurgiia.

Molecular Correlations in Phenylketonuria: Mutation Patterns and Corresponding Biochemical and Clinical Phenotypes in a Heterogeneous California Population

S. Packman, G. Enns, R. Koch, 1999, Pediatric Research.