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Slow retinal degeneration in a mouse model: morphological and functional aspects

Pomeranian Journal of Life Sciences, 2015, Vol.61 (1), p.81-89

2015

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Mutations of noncollagen genes in osteogenesis imperfecta--implications of the gene products in collagen biosynthesis and pathogenesis of disease

Postȩpy higieny i medycyny doświadczalnej, 2012-06, Vol.66, p.359-371

Galicka, Anna

2012

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Genetic aspect of Dupuytren's diseases

Wiadomości lekarskie (1960), 2004, Vol.57 (1-2), p.59

2004

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Familial glucocorticoid deficiency

Pediatric endocrinology, diabetes, and metabolism, 2007, Vol.13 (2), p.91

2007

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Neurodegeneration with brain iron accumulation, type-I (NBIA-I) (formerly Hallervorden-Spatz, disease). Par I: clinical manifestation and treatment

Neurologia i neurochirurgia polska, 2002-09, Vol.36 (5), p.947

Bertrand, Ewa

2002

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Genetic heterogeneity of retinitis pigmentosa

Klinika oczna, 1994-01, Vol.96 (1), p.24

1994

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Problem of hereditary deafness

Otolaryngologia Polska, 1990, Vol.44 (4), p.282-286

1990

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Concepts of heredity in simple psoriasis based on personal studies. I. Simple model - one or two loci

Przegląd dermatologiczny, 1983-07, Vol.70 (4), p.341

1983

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Molecular basis of phenylketonuria

Postępy biochemii, 1990, Vol.36 (3-4), p.24

1990

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Heredity in diseases of the visual system. 1. General laws of genetics

Klinika oczna, 1979-03, Vol.81 (3), p.243

Skubiszewska, T

1979

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Hyperargininemia. Clinical aspects and molecular basis of the defect

Pediatria polska, 1987-04, Vol.62 (4), p.261-272

Konarska, L

1987

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Genetic factors in hemophilia

Acta haematologica polonica, 1987-01, Vol.18 (1-2), p.96

Rozynkowa, D

1987

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Experimental studies on a hereditary central nervous system disease in PT rabbits. V. Clinical syndrome in generations 1-10

Neurologia i neurochirurgia polska, 1975-09, Vol.9 (5), p.569

1975

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Genetic forms of von Willebrand's disease

Acta haematologica polonica, 1982-07, Vol.13 (3-4), p.91

Pniejnia Olszyński, W

1982

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Autosomal and sex-linked heredity

Ginekologia polska, 1972-04, Vol.43 (4), p.501

Boczkowski, K

1972

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Congenital erythroderma ichthyosiforme sicca evaluated from the standpoint of population genetics. I. Approximate determination of the incidence of mutated autosomal recessive gene determining erythroderma ichthyosiforme sicca and the results of its presence in the gene pool of the population in the former province of Bydgoszcz

Przegląd dermatologiczny, 1978-11, Vol.65 (6), p.643

1978

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Regulation of replication of colicinogenic factors

Postȩpy higieny i medycyny doświadczalnej, 1972-09, Vol.26 (5), p.621

Derylo, M

1972

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Congenital erythroderma ichthyosiforme sicca evaluated from the standpoint of population genetics. II. Prognosis of consequences of the presence of the mutated autosomal recessive gene determining congenital erythroderma ichthyosiforme sicca in the population of the former province of Bydgoszcz

Przegląd dermatologiczny, 1978-11, Vol.65 (6), p.649

1978

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Chronic mucocutaneous candidiasis

Przegląd dermatologiczny, 1985-09, Vol.72 (5), p.446

Kadyków, M

1985

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Role of hh-Bombay blood group in the inheritance of serologic characteristics of ABO blood groups system

Wiadomości lekarskie (1960), 1973-11, Vol.26 (21), p.2003

Marcinkowski, T

1973

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Genetic counseling

Pediatria polska, 1976-04, Vol.51 (4), p.455-461

Pietrzyk, J J

1976

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Dermatologic problems in population genetics

Przegląd dermatologiczny, 1975-03, Vol.62 (2), p.265

1975

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Homocystinuria and cystathioninuria

Postȩpy higieny i medycyny doświadczalnej, 1973-09, Vol.27 (5), p.567

1973

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Application of gene and chromosome studies to dermatology

Przegląd dermatologiczny, 1972, Vol.59 (2), p.229

Chodynicka, B

1972

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Heterozygotic form of mucoviscidosis in children

Pediatria polska, 1971, Vol.46 (7), p.825-832

1971

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Slow retinal degeneration in a mouse model: morphological and functional aspects

Mutations of noncollagen genes in osteogenesis imperfecta--implications of the gene products in collagen biosynthesis and pathogenesis of disease

Genetic aspect of Dupuytren's diseases

Familial glucocorticoid deficiency

Neurodegeneration with brain iron accumulation, type-I (NBIA-I) (formerly Hallervorden-Spatz, disease). Par I: clinical manifestation and treatment

Genetic heterogeneity of retinitis pigmentosa

Problem of hereditary deafness

Concepts of heredity in simple psoriasis based on personal studies. I. Simple model - one or two loci

Molecular basis of phenylketonuria

Heredity in diseases of the visual system. 1. General laws of genetics

Hyperargininemia. Clinical aspects and molecular basis of the defect

Genetic factors in hemophilia

Experimental studies on a hereditary central nervous system disease in PT rabbits. V. Clinical syndrome in generations 1-10

Genetic forms of von Willebrand's disease

Autosomal and sex-linked heredity

Regulation of replication of colicinogenic factors

Congenital erythroderma ichthyosiforme sicca evaluated from the standpoint of population genetics. II. Prognosis of consequences of the presence of the mutated autosomal recessive gene determining congenital erythroderma ichthyosiforme sicca in the population of the former province of Bydgoszcz

Chronic mucocutaneous candidiasis

Role of hh-Bombay blood group in the inheritance of serologic characteristics of ABO blood groups system

Genetic counseling

Dermatologic problems in population genetics

Homocystinuria and cystathioninuria

Application of gene and chromosome studies to dermatology

Heterozygotic form of mucoviscidosis in children

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