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Radiation-induced pleomorphic sarcoma with rhabdomyoblastic differentiation of the lower limb following treatment of vaginal squamous cell carcinoma – A case report and review of the literature

Gynecologic oncology reports, 2023-08, Vol.48, p.101201, Article 101201

2023

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Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: A case report and literature review

American journal of medical genetics. Part A, 2015-06, Vol.167A (6), p.1330-1336

2015

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Molecular Characterization of Testicular Mesothelioma and the Role of Asbestos as a Causative Factor

Archives of pathology & laboratory medicine (1976), 2023-12, Vol.147 (12), p.1446-1450

2023

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Reducing Preoperative Fasting Through Technology and Education in an Acute General Surgical Adult Cohort

Joint Commission journal on quality and patient safety, 2023-11, Vol.49 (11), p.584-591

2023

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Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long‐term treatment with subcutaneous protein C concentrate

British journal of haematology, 2016-03, Vol.172 (5), p.811-813

2016

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A case report of dedifferentiated endometrioid carcinoma arising in the ovary and review of flinders medical centre’s experience with mismatch repair immunohistochemistry for screening of lynch syndrome

Pathology, 2017-02, Vol.49, p.S75-S75

2017

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De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review

American journal of medical genetics. Part A, 2013-06, Vol.161A (6), p.1508-1512

2013

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Intrauterine Fetal Death With Vanishing Gastroschisis and Post Mortem Examination Findings

Pediatric and developmental pathology, 2017-04, Vol.20 (2), p.158-162

2017

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CASE REPORT OF INTRAUTERINE FETAL DEATH WITH VANISHING GASTROSCHISIS AND POST MORTEM EXAMINATION FINDINGS

Pediatric and developmental pathology, 2014-12, Article 14-10-1558-CR.1

2014

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Challenging array CGH case involving a duplication of exons 10–18 of the DMD gene in a boy with normal creatinine kinase levels

Pathology, 2013, Vol.45, p.S29-S29

2013

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Hereditary protein C deficiency and thrombosis: two case reports

Pathology, 2013, Vol.45, p.S93-S93

2013

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Microarray is a valuable tool in investigation of fetal autopsy cases with at least one malformation

Pathology, 2012, Vol.44, p.S84-S84

2012

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Radiation-induced pleomorphic sarcoma with rhabdomyoblastic differentiation of the lower limb following treatment of vaginal squamous cell carcinoma - A case report and review of the literature

Gynecologic oncology reports, 2023, Vol.48, p.101201-101201

2023

Volltextzugriff (PDF)

Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long-term treatment with subcutaneous protein C concentrate

British journal of haematology, 2016, Vol.172 (5), p.811-813

2016

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Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

The New England journal of medicine, 2020-10, Vol.383 (18), p.1746-1756

2020

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A Whole-Genome-Based Gene-by-Gene Typing System for Standardized High-Resolution Strain Typing of Bacillus anthracis

Journal of clinical microbiology, 2021-06, Vol.59 (7), p.e0288920-e0288920

2021

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Early posthospitalization recovery after extracorporeal membrane oxygenation in survivors of COVID-19

The Journal of thoracic and cardiovascular surgery, 2023-09, Vol.166 (3), p.842-851.e1

2023

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Erratum: Development and implementation of a Core Genome Multilocus Sequence Typing (cgMLST) scheme for Haemophilus influenzae

Microbial genomics, 2024-10, Vol.10 (10)

2024

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Development and implementation of a core genome multilocus sequence typing scheme for Haemophilus influenzae

Microbial genomics, 2024-08, Vol.10 (8)

2024

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Common variants near MC4R are associated with fat mass, weight and risk of obesity

Nature genetics, 2008-06, Vol.40 (6), p.768-775

2008

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Clinical and epidemiological correlates of treatment change in patients with NMOSD: insights from the CIRCLES cohort

Journal of neurology, 2023-04, Vol.270 (4), p.2048-2058

2023

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Long-term recovery of survivors of coronavirus disease (COVID-19) treated with extracorporeal membrane oxygenation: The next imperative

JTCVS open, 2021-03, Vol.5, p.163-168

2021

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Rejuvenation of RBCs: validation of a manufacturing method suitable for clinical use

Transfusion (Philadelphia, Pa.), 2019-09, Vol.59 (9), p.2952-2963

2019

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Assessment of the urgency and deferability of transfusion to inform emergency blood planning and triage: the Bloodhound prospective audit of red blood cell use

Transfusion (Philadelphia, Pa.), 2009-11, Vol.49 (11), p.2296-2303

2009

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An adverse event screening tool based on routinely collected hospital-acquired diagnoses

International journal for quality in health care, 2012-06, Vol.24 (3), p.266-278

2012

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Radiation-induced pleomorphic sarcoma with rhabdomyoblastic differentiation of the lower limb following treatment of vaginal squamous cell carcinoma – A case report and review of the literature

Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: A case report and literature review

Molecular Characterization of Testicular Mesothelioma and the Role of Asbestos as a Causative Factor

Reducing Preoperative Fasting Through Technology and Education in an Acute General Surgical Adult Cohort

Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long‐term treatment with subcutaneous protein C concentrate

A case report of dedifferentiated endometrioid carcinoma arising in the ovary and review of flinders medical centre’s experience with mismatch repair immunohistochemistry for screening of lynch syndrome

De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review

Intrauterine Fetal Death With Vanishing Gastroschisis and Post Mortem Examination Findings

CASE REPORT OF INTRAUTERINE FETAL DEATH WITH VANISHING GASTROSCHISIS AND POST MORTEM EXAMINATION FINDINGS

Challenging array CGH case involving a duplication of exons 10–18 of the DMD gene in a boy with normal creatinine kinase levels

Hereditary protein C deficiency and thrombosis: two case reports

Microarray is a valuable tool in investigation of fetal autopsy cases with at least one malformation

Radiation-induced pleomorphic sarcoma with rhabdomyoblastic differentiation of the lower limb following treatment of vaginal squamous cell carcinoma - A case report and review of the literature

Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long-term treatment with subcutaneous protein C concentrate

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

A Whole-Genome-Based Gene-by-Gene Typing System for Standardized High-Resolution Strain Typing of Bacillus anthracis

Early posthospitalization recovery after extracorporeal membrane oxygenation in survivors of COVID-19

Erratum: Development and implementation of a Core Genome Multilocus Sequence Typing (cgMLST) scheme for Haemophilus influenzae

Development and implementation of a core genome multilocus sequence typing scheme for Haemophilus influenzae

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Clinical and epidemiological correlates of treatment change in patients with NMOSD: insights from the CIRCLES cohort

Long-term recovery of survivors of coronavirus disease (COVID-19) treated with extracorporeal membrane oxygenation: The next imperative

Rejuvenation of RBCs: validation of a manufacturing method suitable for clinical use

Assessment of the urgency and deferability of transfusion to inform emergency blood planning and triage: the Bloodhound prospective audit of red blood cell use

An adverse event screening tool based on routinely collected hospital-acquired diagnoses

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