A familial case of alveolar capillary dysplasia with misalignment of the pulmonary veins: the clinicopathological features and unusual glomeruloid endothelial proliferation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1746-1596
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
A familial case of alveolar capillary dysplasia with misalignment of the pulmonary veins: the clinicopathological features and unusual glomeruloid endothelial proliferation ; volume:15 ; number:1 ; day:9 ; month:5 ; year:2020 ; pages:1-7 ; date:12.2020
Diagnostic pathology ; 15, Heft 1 (9.5.2020), 1-7, 12.2020
- Creator
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Kitano, Akiko
Nakaguro, Masato
Tomotaki, Seiichi
Hanaoka, Shintaro
Kawai, Masahiko
Saito, Akiko
Hayakawa, Masahiro
Takahashi, Yoshiyuki
Kawasaki, Hidenori
Yamada, Takahiro
Ikeda, Masahiko
Onda, Tetsuo
Cho, Kazutoshi
Haga, Hironori
Nakazawa, Atsuko
Minamiguchi, Sachiko
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13000-020-00972-6
- URN
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urn:nbn:de:101:1-2020071621063069896539
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:58 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kitano, Akiko
- Nakaguro, Masato
- Tomotaki, Seiichi
- Hanaoka, Shintaro
- Kawai, Masahiko
- Saito, Akiko
- Hayakawa, Masahiro
- Takahashi, Yoshiyuki
- Kawasaki, Hidenori
- Yamada, Takahiro
- Ikeda, Masahiko
- Onda, Tetsuo
- Cho, Kazutoshi
- Haga, Hironori
- Nakazawa, Atsuko
- Minamiguchi, Sachiko
- SpringerLink (Online service)
Other Objects (12)
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The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins
Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype
A Morphomolecular Approach to Alveolar Capillary Dysplasia
Genotype–phenotype correlation in two Polish neonates with alveolar capillary dysplasia
Identification of endothelial and mesenchymal FOXF1 enhancers involved in alveolar capillary dysplasia
Coexistence of craniopharyngioma and cranial fibrous dysplasia: a case series of clinicopathological study
Of the Veins
Enlarged jugular veins
Axion misalignment driven to the bottom
Dynamical axion misalignment with small instantons
Axion dark matter from frictional misalignment
Alveolar capillary dysplasia with misalignment of pulmonary veins in a premature newborn: the role of lung ultrasound
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins
Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype
A Morphomolecular Approach to Alveolar Capillary Dysplasia
Genotype–phenotype correlation in two Polish neonates with alveolar capillary dysplasia
Identification of endothelial and mesenchymal FOXF1 enhancers involved in alveolar capillary dysplasia
Coexistence of craniopharyngioma and cranial fibrous dysplasia: a case series of clinicopathological study
Of the Veins
Enlarged jugular veins
Axion misalignment driven to the bottom
Dynamical axion misalignment with small instantons
Axion dark matter from frictional misalignment
Alveolar capillary dysplasia with misalignment of pulmonary veins in a premature newborn: the role of lung ultrasound
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins
Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype
A Morphomolecular Approach to Alveolar Capillary Dysplasia
Genotype–phenotype correlation in two Polish neonates with alveolar capillary dysplasia
Identification of endothelial and mesenchymal FOXF1 enhancers involved in alveolar capillary dysplasia
Coexistence of craniopharyngioma and cranial fibrous dysplasia: a case series of clinicopathological study
Of the Veins
Enlarged jugular veins
Axion misalignment driven to the bottom
Dynamical axion misalignment with small instantons