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Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2011-11, Vol.22 (11), p.2047-2056

2011

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Mirror Syndrome: A Systematic Review of Fetal Associated Conditions, Maternal Presentation and Perinatal Outcome

Fetal diagnosis and therapy, 2010-01, Vol.27 (4), p.191-203

2010

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Abnormal vascular architecture at the placental-maternal interface in placenta increta

American journal of obstetrics and gynecology, 2012-09, Vol.207 (3), p.188.e1-188.e9

2012

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Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene ( ACTA1 ) mutation

Neuromuscular disorders : NMD, 2010-08, Vol.20 (8), p.531-533

2010

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Transgenic mice expressing small interfering RNA against Gata4 point to a crucial role of Gata4 in the heart and gonads

Journal of molecular endocrinology, 2009-10, Vol.43 (4), p.157-169

2009

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The CD34 epitope is expressed in neoplastic and malformative lesions associated with chronic, focal epilepsies

Acta neuropathologica, 1999-05, Vol.97 (5), p.481-490

1999

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Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis

Journal of rheumatology, 2004-12, Vol.31 (12), p.2519

2004

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Changing expression of cyclooxygenases and prostaglandin receptor EP4 during development of the human ductus arteriosus

Pediatric research, 2006-09, Vol.60 (3), p.270-275

2006

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Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4

Human genetics, 2022-11, Vol.141 (11), p.1785-1794

2022

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Partial hydatidiform mole with extensive angiomatoid vessel configuration in a first trimester miscarriage

International journal of gynecological pathology, 2015-05, Vol.34 (3), p.253

2015

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The transcription factor Ets-1 is expressed in human amniochorionic membranes and is up-regulated in term and preterm premature rupture of membranes

Journal of perinatal medicine, 2005-01, Vol.33 (4), p.314-319

2005

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Aberrant right subclavian artery as a new cardiac sign in second- and third-trimester fetuses with Down syndrome

American journal of obstetrics and gynecology, 2005, Vol.192 (1), p.257-263

2005

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Novel Insights in Fetal Cardiomyopathy due to in utero Herpes Simplex Virus Infection

Fetal diagnosis and therapy, 2017-10, Vol.42 (3), p.236-239

2017

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Clinical, Laboratory, and Placental Findings in Perinatal Listeriosis

Fetal and pediatric pathology, 2016-09, Vol.35 (5), p.307-314

2016

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The Expression of VEGF and its Receptors in the Human Ductus Arteriosus

Pediatric research, 2008-10, Vol.64 (4), p.340-345

2008

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Three-Dimensional Multi-Slice View: New Prospects for Evaluation of Congenital Anomalies in the Fetus

Journal of ultrasound in medicine, 2006-08, Vol.25 (8), p.1041-1049

2006

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The expression of vascular endothelial growth factor and its receptors in congenital bronchopulmonary cystic malformations

European journal of pediatric surgery, 2012-04, Vol.22 (2), p.127-132

2012

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Spontaneous regression of a vascular tumor of the skull base--infantile hemangioendothelioma?

Journal of pediatric hematology/oncology, 2008-09, Vol.30 (9), p.712-715

2008

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Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis

Prenatal diagnosis, 2007-05, Vol.27 (5), p.475-478

2007

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Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13

Prenatal diagnosis, 2006-03, Vol.26 (3), p.273-276

2006

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Three‐Dimensional Multi‐Slice View

Journal of ultrasound in medicine, 2006-08, Vol.25 (8), p.1041-1049

2006

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Detection of infectious colitis by 18F-fluorodeoxyglucose-positron emission tomography in a child receiving intensive care after cardiac surgery

Pediatric radiology, 2005-07, Vol.35 (7), p.702-705

2005

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Unusual mesoblastic nephroma in a young child

Pediatric radiology, 2003, Vol.33 (1), p.62-65

2003

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Diagnostic dilemma with elevated level of α-fetoprotein in an undiagnosed twin pregnancy with a small discordant holoacardius acephalus

American journal of obstetrics and gynecology, 1997-08, Vol.177 (2), p.466-468

1997

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Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis

Prenatal Diagnosis, 2007, Vol.27 (5), p.475-478

2007

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Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

Mirror Syndrome: A Systematic Review of Fetal Associated Conditions, Maternal Presentation and Perinatal Outcome

Abnormal vascular architecture at the placental-maternal interface in placenta increta

Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene ( ACTA1 ) mutation

Transgenic mice expressing small interfering RNA against Gata4 point to a crucial role of Gata4 in the heart and gonads

The CD34 epitope is expressed in neoplastic and malformative lesions associated with chronic, focal epilepsies

Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis

Changing expression of cyclooxygenases and prostaglandin receptor EP4 during development of the human ductus arteriosus

Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4

Partial hydatidiform mole with extensive angiomatoid vessel configuration in a first trimester miscarriage

The transcription factor Ets-1 is expressed in human amniochorionic membranes and is up-regulated in term and preterm premature rupture of membranes

Aberrant right subclavian artery as a new cardiac sign in second- and third-trimester fetuses with Down syndrome

Novel Insights in Fetal Cardiomyopathy due to in utero Herpes Simplex Virus Infection

Clinical, Laboratory, and Placental Findings in Perinatal Listeriosis

The Expression of VEGF and its Receptors in the Human Ductus Arteriosus

Three-Dimensional Multi-Slice View: New Prospects for Evaluation of Congenital Anomalies in the Fetus

The expression of vascular endothelial growth factor and its receptors in congenital bronchopulmonary cystic malformations

Spontaneous regression of a vascular tumor of the skull base--infantile hemangioendothelioma?

Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis

Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13

Three‐Dimensional Multi‐Slice View

Detection of infectious colitis by 18F-fluorodeoxyglucose-positron emission tomography in a child receiving intensive care after cardiac surgery

Unusual mesoblastic nephroma in a young child

Diagnostic dilemma with elevated level of α-fetoprotein in an undiagnosed twin pregnancy with a small discordant holoacardius acephalus

Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis

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