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Influence of human Papilloma Virus (hPV) infection on early pregnancy

Ginekologia polska, 2019-01, Vol.90 (2), p.72-75

2019

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Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes

Journal of clinical medicine, 2022-03, Vol.11 (6), p.1513

2022

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Cases of tetrasomy 9p and trisomy 9p in prenatal diagnosis—Analysis of noninvasive and invasive test results

Frontiers in genetics, 2022-09, Vol.13, p.994455-994455

2022

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Streptococcus mutans in the oral cavity as a risk factor for threatened miscarriage

Ginekologia polska, 2024-01, Vol.95 (2), p.123-125

2024

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Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome

Journal of genetic counseling, 2024-08, Vol.33 (4), p.927-930

2024

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Bartter[StQuote]s syndrome as a forgotten cause of polyhydramnios

European journal of obstetrics & gynecology and reproductive biology, 2024-02, Vol.293, p.58

2024

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Ultrasound and echocardiographic findings obtained in the second and third trimesters of gestation in fetuses with normal karyotype and increased nuchal translucency

Journal of ultrasonography, 2013-03, Vol.13 (52), p.21-30

2013

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The impact of the COVID-19 pandemic on the course of miscarriages

Ginekologia polska, 2024-01, Vol.95 (1), p.62-66

2024

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2150-PUB: Chemotactic Cytokine Receptor 5 (CCR5) Gene Promoter Polymorphism (rs1799987) Is Associated with the Risk of Diabetic Kidney Disease in Polish Patients with Type 2 Diabetes

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

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Prenatal karyotype results from 2169 invasive tests

Ginekologia polska, 2023-01, Vol.94 (11), p.918-921

2023

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Prenatal Sonographic Features of Rare Chromosome 13 Aberrations

Application of clinical genetics, 2022-10, Vol.15, p.145-151

2022

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Conservative treatment of abnormally located intrauterine pregnancies (cervical and cesarean scar pregnancies): a multicenter analysis (Polish series)

The journal of maternal-fetal & neonatal medicine, 2020-03, Vol.33 (6), p.993-998

2020

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Prenatal diagnosis of agenesis of corpus callosum

European journal of obstetrics & gynecology and reproductive biology, 2016-11, Vol.206, p.e52-e52

2016

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Early ultrasound diagnosis of diastrophic dysplasia in the first trimester of pregnancy

European journal of obstetrics & gynecology and reproductive biology, 2016-11, Vol.206, p.e78-e78

2016

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Parkinson's disease gene therapy: a comparative effectiveness review of completed clinical trials in terms of their possible implementation in treatment

Medical Science Pulse, 2023-02, Vol.16 (4), p.1-7

2023

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Occurrence of c.976 G>T (p.Val326Leu) and c.452 G>A (p.Trp151Ter) variants in DHCR7 gene in population of polish women with recurrent miscarriage

European journal of obstetrics & gynecology and reproductive biology, 2020-09, Vol.252, p.252-255

2020

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The absence of fetal nasal bones in ultrasound examination between 11 + 0 and 13 + 6 weeks of gestation versus the occurrence of trisomies 21, 18, and 13

Ginekologia polska, 2019-01, Vol.90 (10), p.604-606

2019

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Prenatal diagnosis of Goldenhar syndrome – case report

European journal of obstetrics & gynecology and reproductive biology, 2016-11, Vol.206, p.e26-e26

2016

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Prenatal Diagnosis of Holt-Oram Syndrome

Kardiologia prenatalna echo płodu, 2015-03, Vol.5 (1), p.29-32

2015

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Association of single nucleotide polymorphism (rs741301) of the ELMO1 gene with diabetic kidney disease in Polish patients with type 2 diabetes: a pilot study

Endokrynologia polska, 2020-01, Vol.71 (1), p.66-72

2020

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Genetic causes of recurrent miscarriages

Ginekologia polska, 2016-01, Vol.87 (10), p.722-726

2016

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Cell-free fetal DNA testing in prenatal diagnosis: Recommendations of the Polish Gynecological Society and the Polish Human Genetics Society

European journal of obstetrics & gynecology and reproductive biology, 2017-07, Vol.214, p.190-191

2017

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Is genetic testing required in a child with an ovarian germ cell tumour?

Pediatria polska, 2019, Vol.94 (2), p.140-144

2019

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DORV in fetuses: how to consult future parents at a prenatal cardiology center? Retrospective analysis of 39 cases

Kardiologia prenatalna echo płodu, 2014-09, Vol.4 (3), p.13-17

2014

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Influence of human Papilloma Virus (hPV) infection on early pregnancy

Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes

Cases of tetrasomy 9p and trisomy 9p in prenatal diagnosis—Analysis of noninvasive and invasive test results

Streptococcus mutans in the oral cavity as a risk factor for threatened miscarriage

Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome

Bartter[StQuote]s syndrome as a forgotten cause of polyhydramnios

Ultrasound and echocardiographic findings obtained in the second and third trimesters of gestation in fetuses with normal karyotype and increased nuchal translucency

The impact of the COVID-19 pandemic on the course of miscarriages

2150-PUB: Chemotactic Cytokine Receptor 5 (CCR5) Gene Promoter Polymorphism (rs1799987) Is Associated with the Risk of Diabetic Kidney Disease in Polish Patients with Type 2 Diabetes

Prenatal karyotype results from 2169 invasive tests

Prenatal Sonographic Features of Rare Chromosome 13 Aberrations

Conservative treatment of abnormally located intrauterine pregnancies (cervical and cesarean scar pregnancies): a multicenter analysis (Polish series)

Prenatal diagnosis of agenesis of corpus callosum

Early ultrasound diagnosis of diastrophic dysplasia in the first trimester of pregnancy

Parkinson's disease gene therapy: a comparative effectiveness review of completed clinical trials in terms of their possible implementation in treatment

Occurrence of c.976 G>T (p.Val326Leu) and c.452 G>A (p.Trp151Ter) variants in DHCR7 gene in population of polish women with recurrent miscarriage

The absence of fetal nasal bones in ultrasound examination between 11 + 0 and 13 + 6 weeks of gestation versus the occurrence of trisomies 21, 18, and 13

Prenatal diagnosis of Goldenhar syndrome – case report

Prenatal Diagnosis of Holt-Oram Syndrome

Association of single nucleotide polymorphism (rs741301) of the ELMO1 gene with diabetic kidney disease in Polish patients with type 2 diabetes: a pilot study

Genetic causes of recurrent miscarriages

Recommendations for prenatal diagnostics of the Polish Society of Gynaecologists and Obstetricians and the Polish Society of Human Genetics

Cell-free fetal DNA testing in prenatal diagnosis: Recommendations of the Polish Gynecological Society and the Polish Human Genetics Society

Is genetic testing required in a child with an ovarian germ cell tumour?

DORV in fetuses: how to consult future parents at a prenatal cardiology center? Retrospective analysis of 39 cases

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