Zobrazeno 1 - 10 of 128 pro vyhledávání: '"M. H. Witte"'
1
Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a
Autor: X, Geng, L, Chen, R S, Srinivasan, R J, Kylat, M H, Witte, R J, Erickson
Publikováno v: Lymphology. 55(3)
We have studied the lymphatic phenotypes of 2 mutations, known to cause abnormalities of lymphatics in humans, in mice. The
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3685f7f227a85c8fb444e3ffe27ec5a4
https://pubmed.ncbi.nlm.nih.gov/36446400
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2
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation
Autor: D J, Mustacich, R I, Kylat, M J, Bernas, R J, Myles, J A, Jones, J D, Kanady, A M, Simon, T G, Georgieva, M H, Witte, R P, Erickson, P W, Pires
Publikováno v: Lymphology. 54(2)
Connexin proteins form gap junctions controlling exchange of ions and small molecules between cells and play an important role in movement of lymph within lymphatic vessels. Connexin47 (CX47) is highly expressed in lymphatic endothelial cells and CX4
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f61b25456adf58a6b843ad12493b4d28
https://pubmed.ncbi.nlm.nih.gov/34735753
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3
Imaging of lymphatic dysplasia in Noonan syndrome: Case studies and historical atlas
Autor: T, Cox, C, Vance, S, Daley, C, Papendieck, H, McGregor, P H, Kuo, M H, Witte
Publikováno v: Lymphology. 54(1)
To determine the historical use and utility of various lymphatic imaging modalities in Noonan syndrome (NS) patients, we performed a comprehensive literature review by collecting the published medical imaging of NS lymphatic dysplasias. We correlated
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b1a50ec6df1818505c0a2567f1bcc066
https://pubmed.ncbi.nlm.nih.gov/34506085
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4
SARS-CoV-2/COVID-19, Lymphatic vessels, lymph, and lymphology
Autor: M H, Witte, S K, Daley
Publikováno v: Lymphology. 53(3)
[Editorial] Lymphatic vessels and lymph are a missing link in SARS-CoV-2/COVID-19 pathophysiology and therapeutic strategies. Based on well-established principles of lymphatic function and dysfunction and a neglected literature, this article highligh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::047cf92b340aab84e84ac6bfe6c7f2c1
https://pubmed.ncbi.nlm.nih.gov/33350283
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5
Thoracic duct decompression: An idea whose time has come - again
Autor: M H, Witte
Publikováno v: Lymphology. 53(2)
[Editorial] Thoracic duct decompression (TDD) is an idea first proposed and applied as a novel therapeutic strategy by lymphologists in the 1960's. TDD is recently being reexamined and, in selected patients with portal hypertension from hepatic cirrh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b4990a57b86783265aba57178315b9c2
https://pubmed.ncbi.nlm.nih.gov/33190431
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6
EVOLUTION OF THE 2020 INTERNATIONAL SOCIETY OF LYMPHOLOGY CONSENSUS DOCUMENT PARALLELS ADVANCES IN LYMPHOLOGY: AN HISTORICAL PERSPECTIVE
Autor: M H, Witte, M J, Bernas
Publikováno v: Lymphology. 53(1)
[Editorial] Evolution of the 2020 international society of lymphology consensus document parallels advances in lymphology: An historical perspective.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b70c9c6de1643fd6d7458fa09e319389
https://pubmed.ncbi.nlm.nih.gov/32521125
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7
Whole-body lymphangioscintigraphy and SPECT/CT in children with lymphatic complications after surgery for complex congenital heart disease
Autor: P H, Kuo, B J, Barber, R I, Kylat, S E, Klewer, S, Behan, S, Lau-Braunhut, M J, Bernas, L, Moedano, A D, Bedrick, D J, Mustacich, M H, Witte
Publikováno v: Lymphology. 52(4)
The number of patients surviving repair of complex congenital heart disease (CCHD) has increased due to improved surgical techniques, post operative management and outpatient care. Likewise, this growing patient population has demonstrated an increas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0d8bd618ec5a0f44ee577e6d424a2e52
https://pubmed.ncbi.nlm.nih.gov/32171182
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9
From childhood onset lymphedema to fatal fetal hydrops: Possible modifying genes for a FOXC2 mutation
Autor: L W, Lai, R P, Erickson, M, Bernas, M H, Witte
Publikováno v: Lymphology. 51(2)
We performed whole exome sequencing in a family with FOXC2 mutation where the phenotype in one generation was strikingly more severe. Although there were 3 mutations shared by 2 fatal fetal hydrops cases and not the mildly affected mother, none of th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::43a9fd4702f0d1083bfcf0e136bdb0ca
https://pubmed.ncbi.nlm.nih.gov/30253460
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10
Lymphangioleiomyomatosis and Gorham-Stout disease: Primary or secondary disorders of the lymphatic system?
Autor: M H, Witte
Publikováno v: Lymphology. 50(3)
Lymphangioleimyomatosis and Gorham- Stout disease, rare disorders which share features of proliferating lymphatic vessels, predominantly in the lung in the former and bone in the latter, commonly manifest as progressive lung disease often associated
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d60106b3d2644138141b48c8a6c38f09
https://pubmed.ncbi.nlm.nih.gov/30234247
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