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Placental Pathology Findings during and after SARS-CoV-2 Infection: Features of Villitis and Malperfusion

Pathobiology (Basel), 2021-01, Vol.88 (1), p.69-77

2021

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Exome sequencing of fetal anomaly syndromes: novel phenotype-genotype discoveries

European journal of human genetics : EJHG, 2019-05, Vol.27 (5), p.730-737

2019

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Perfusion-Based Bioreactor Culture and Isothermal Microcalorimetry for Preclinical Drug Testing with the Carbonic Anhydrase Inhibitor SLC-0111 in Patient-Derived Neuroblastoma

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3128

2022

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Pathologic findings of the placenta and clinical implications - recommendations for placental examination

Swiss medical weekly, 2024-10, Vol.154 (10), p.3929

2024

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Bladder Neoplasia in Pediatric Patients-A Single-Center Experience Including a Case Series

Children (Basel), 2023-09, Vol.10 (10), p.1596

2023

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Bone marrow edema pattern in osteoarthritic knees: correlation between MR imaging and histologic findings

Radiology, 2000-06, Vol.215 (3), p.835-840

2000

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Gastrointestinal neuromuscular pathology: guidelines for histological techniques and reporting on behalf of the Gastro 2009 International Working Group

Acta neuropathologica, 2009-08, Vol.118 (2), p.271-301

2009

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Painless swelling of the forefoot and recurrent subcutaneous abscesses of the lower leg-Two distinct presentations illustrating the spectrum of eumycetoma in a nonendemic country

PLoS neglected tropical diseases, 2017-04, Vol.11 (4), p.e0005360-e0005360

2017

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The RNA-Binding Protein RBM3 Is Required for Cell Proliferation and Protects Against Serum Deprivation-Induced Cell Death

Pediatric research, 2010, Vol.67 (1), p.35-41

2010

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Dosage-Dependent Effects of Akt1/Protein Kinase Bα (PKBα) and Akt3/PKBγ on Thymus, Skin, and Cardiovascular and Nervous System Development in Mice

Molecular and Cellular Biology, 2005-12, Vol.25 (23), p.10407-10418

2005

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Juvenile xanthogranuloma involving concurrent iris and skin: Clinical, pathological and molecular pathological evaluations

American journal of ophthalmology case reports, 2018-03, Vol.9 (C), p.10-13

2018

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Morphologic and molecular characterization of renal cell carcinoma in children and young adults

The American journal of surgical pathology, 2004-09, Vol.28 (9), p.1117-1132

2004

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Post-mortem magnetic resonance imaging with computed tomography-guided biopsy for foetuses and infants: a prospective, multicentre, cross-sectional study

BMC pediatrics, 2022-08, Vol.22 (1), p.1-464, Article 464

2022

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Identification of Molecular Tumor Markers in Renal Cell Carcinomas with TFE3 Protein Expression by RNA Sequencing

Neoplasia (New York, N.Y.), 2013-11, Vol.15 (11), p.1231-1240

2013

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Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1178-n/a

2020

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Congenital orbital teratoma: A clinicopathologic case report

American journal of ophthalmology case reports, 2022-06, Vol.26, p.101420, Article 101420

2022

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The histopathology of gastrointestinal motility disorders in children

Seminars in pediatric surgery, 2009-11, Vol.18 (4), p.206-211

2009

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Vascular lesions of bone in children, adolescents, and young adults. A clinicopathologic reappraisal and application of the ISSVA classification

Virchows Archiv : an international journal of pathology, 2009-02, Vol.454 (2), p.161-179

2009

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Morphologic and GATA1 sequencing analysis of hematopoiesis in fetuses with trisomy 21

Human pathology, 2014-05, Vol.45 (5), p.1003-1009

2014

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Is primary chronic osteomyelitis a uniform disease? Proposal of a classification based on a retrospective analysis of patients treated in the past 30 years

Journal of cranio-maxillo-facial surgery, 2004-02, Vol.32 (1), p.43-50

2004

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Vaskuläre Läsionen des Skeletts – Pathologie und Genetik

Osteologie, 2019-02, Vol.28 (1), p.91-97

2019

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Current concepts of enzyme histochemistry in modern pathology

Pathobiology (Basel), 2008-01, Vol.75 (4), p.233-243

2008

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Dual independent genetic etiologies in a lethal complex malformation phenotype

Ultraschall in der Medizin, 2020-04, Vol.41 (2), p.112-114

2020

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A novel homozygous splice‐site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle development

Prenatal diagnosis, 2017-07, Vol.37 (7), p.720-724

2017

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Placental Pathology Findings during and after SARS-CoV-2 Infection: Features of Villitis and Malperfusion

Exome sequencing of fetal anomaly syndromes: novel phenotype-genotype discoveries

Perfusion-Based Bioreactor Culture and Isothermal Microcalorimetry for Preclinical Drug Testing with the Carbonic Anhydrase Inhibitor SLC-0111 in Patient-Derived Neuroblastoma

Pathologic findings of the placenta and clinical implications - recommendations for placental examination

Bladder Neoplasia in Pediatric Patients-A Single-Center Experience Including a Case Series

Bone marrow edema pattern in osteoarthritic knees: correlation between MR imaging and histologic findings

Gastrointestinal neuromuscular pathology: guidelines for histological techniques and reporting on behalf of the Gastro 2009 International Working Group

Painless swelling of the forefoot and recurrent subcutaneous abscesses of the lower leg-Two distinct presentations illustrating the spectrum of eumycetoma in a nonendemic country

The RNA-Binding Protein RBM3 Is Required for Cell Proliferation and Protects Against Serum Deprivation-Induced Cell Death

Dosage-Dependent Effects of Akt1/Protein Kinase Bα (PKBα) and Akt3/PKBγ on Thymus, Skin, and Cardiovascular and Nervous System Development in Mice

Juvenile xanthogranuloma involving concurrent iris and skin: Clinical, pathological and molecular pathological evaluations

Morphologic and molecular characterization of renal cell carcinoma in children and young adults

Post-mortem magnetic resonance imaging with computed tomography-guided biopsy for foetuses and infants: a prospective, multicentre, cross-sectional study

Identification of Molecular Tumor Markers in Renal Cell Carcinomas with TFE3 Protein Expression by RNA Sequencing

Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly

Congenital orbital teratoma: A clinicopathologic case report

The histopathology of gastrointestinal motility disorders in children

Vascular lesions of bone in children, adolescents, and young adults. A clinicopathologic reappraisal and application of the ISSVA classification

Morphologic and GATA1 sequencing analysis of hematopoiesis in fetuses with trisomy 21

Neuroblastoma tumorigenesis is regulated through the Nm23-H1/h-Prune C-terminal interaction

Is primary chronic osteomyelitis a uniform disease? Proposal of a classification based on a retrospective analysis of patients treated in the past 30 years

Vaskuläre Läsionen des Skeletts – Pathologie und Genetik

Current concepts of enzyme histochemistry in modern pathology

Dual independent genetic etiologies in a lethal complex malformation phenotype

A novel homozygous splice‐site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle development

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