Znaleziono wyników: 3

Liczba wyników na stronie

Wyniki wyszukiwania

Sortuj według:

Ogranicz wyniki do:

Frequency of mutations related to hereditary haemochromatosis in northwestern Poland

100%

Raszeja-Wyszomirska J., Kurzawski G., Suchy J., Zawada I., Lubinski J., Milkiewicz P.

Journal of Applied Genetics

2008

tom 49

nr 1

105-107

Hereditary haemochromatosis has been linked with C282Y and H63D mutations of the HFE gene. In Europe, frequencies of these mutations are the highest in Northern European countries and gradually decrease southwards. We analysed the prevalence of HFE mutations in 1517 DNA samples, including 1000 samples from the general population (subjects registered at general practitioner practices) in northwestern Poland, and 517 samples of cord blood from the same region. We identified 2 (0.13%) homozygotes and 117 (7.8%) heterozygotes for the C282Y mutation. As regards the H63D mutation (1505 DNA samples analysed), 38 (2.5%) samples were homozygotes and 380 (25%) were heterozygotes. Twenty-one (1.4%) compound heterozygotes were found. These results correspond well with data from other Central European countries and seem to confirm the hypothesis of North-South spread of the C282Y mutation.

The effect of short term treatment with probiotic VSL#3 on various clinical and biochemical parameters in patients with liver cirrhosis

84%

Marlicz W., Wunsch E., Mydlowska M., Milkiewicz M., Serwin K., Mularczyk M., Milkiewicz P., Raszeja-Wyszomirska J.

Journal of Physiology and Pharmacology

2016

tom 67

nr 6

Apolipoprotein E4 allele is associated with substantial changes in the plasma lipids and hyaluronic acid content in patients with nonalcoholic fatty liver disease

68%

Stachowska E., Maciejewska D., Ossowski P., Drozd A., Ryterska K., Banaszczak M., Milkiewicz M., Raszeja-Wyszomirska J., Slebioda M., Milkiewicz P., Jelen H.

Journal of Physiology and Pharmacology

2013

tom 64

nr 6

Ograniczanie wyników

2 Journal of Physiology and Pharmacology

1 Journal of Applied Genetics

3 Milkiewicz P.

3 Raszeja-Wyszomirska J.

2 Milkiewicz M.

1 Banaszczak M.

1 Drozd A.

1 Jelen H.

1 Kurzawski G.

1 Lubinski J.

1 Maciejewska D.

1 Marlicz W.

1 Mularczyk M.

1 Mydlowska M.

1 Ossowski P.

1 Ryterska K.

1 Serwin K.

1 Slebioda M.

1 Stachowska E.

1 Suchy J.

1 Wunsch E.

1 Zawada I.

1 2016

1 2013

1 2008

Wyniki wyszukiwania

Frequency of mutations related to hereditary haemochromatosis in northwestern Poland

The effect of short term treatment with probiotic VSL#3 on various clinical and biochemical parameters in patients with liver cirrhosis

Apolipoprotein E4 allele is associated with substantial changes in the plasma lipids and hyaluronic acid content in patients with nonalcoholic fatty liver disease