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99641 |
An unusual case of the congenital mesenchymal hamartoma of the neck associated with the midline cervical cleft in neonate
Enthalten in Case reports in perinatal medicine Bd. 11, 2022, Nr. 1. 04 S.
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99642 |
Autoimmune polyglandular syndrome type 2 in pregnancy: a case report and review of the literature
Enthalten in Case reports in perinatal medicine Bd. 11, 2022, Nr. 1. 04 S.
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99643 |
Challenges in genetic counseling for congenital anomalies of the kidneys and urinary tract (CAKUT) spectrum
Enthalten in Case reports in perinatal medicine Bd. 11, 2022, Nr. 1. 06 S.
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99644 |
Frequency and Clinical Significance Anti-PS/PT Antibodies in Patients with Antiphospholipid Syndrome – Single Centre Observational Study in the United Kingdom
Enthalten in Seminars in thrombosis and hemostasis 01.11.2022
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99645 |
LPL Gene Mutation in Type 1 Familial Triglyceridemia Presenting as Recurrent Pancreatitis and Complicated by COVID19
Enthalten in Journal of pediatric genetics 01.11.2022
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99646 |
Multimodal postpartum imaging of a severe case of Couvelaire uterus
Enthalten in Case reports in perinatal medicine Bd. 11, 2022, Nr. 1. 05 S.
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99647 |
Orthostatic intolerance and neurocognitive impairment in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
Enthalten in Epidemiologic methods Bd. 11, 2022, Nr. 1. 9 S.
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99648 |
Prenatal diagnosis of ectrodactyly-ectodermal dysplasia clefting syndrome ‒ a case report with literature review
Enthalten in Case reports in perinatal medicine Bd. 11, 2022, Nr. 1. 05 S.
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99649 |
Selection bias and multiple inclusion criteria in observational studies
Enthalten in Epidemiologic methods Bd. 11, 2022, Nr. 1. 21 S.
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99650 |
Umbilical artery aneurysm without aneuploidy and delivery of a live neonate
Enthalten in Case reports in perinatal medicine Bd. 11, 2022, Nr. 1. 05 S.
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