Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Susanne Mackensen-Haen"'
Autor:
Sebastian Peter, Haen, Rebekka, Mannal, Martin, Steeg, Peter, Seizer, Michaela, Rockenstiehl, Susanne, Mackensen-Haen, Marius, Horger, Lothar, Kanz, Wichard, Vogel
Publikováno v:
Deutsche medizinische Wochenschrift (1946). 141(9)
We report the case of a 59-year-old male who was admitted to hospital with acute chest pain. Coronary heart disease was known from the medical history. The patient reported recurrent ostealgia and susceptibility for infection during the last months b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a71c7bcab1efe26132631475939d6d5c
https://pubmed.ncbi.nlm.nih.gov/27123729
https://pubmed.ncbi.nlm.nih.gov/27123729
Autor:
Gabriele Meyberg-Solomayer, Karl Oliver Kagan, Susanne Mackensen-Haen, Markus Wallwiener, Sarah Schott
Publikováno v:
Archives of Gynecology and Obstetrics. 280:293-296
Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95d1df5db64fee6d1a41536f9f768954
https://doi.org/10.1007/s00404-008-0880-4
https://doi.org/10.1007/s00404-008-0880-4
Autor:
Herbert Enders, Thomas Eggermann, Heidemarie Kendziorra, Peter Kaiser, Ulrike A. Mau, Susanne Mackensen-Haen, Ludger Sieverding, Ute Klein-Vogler
Publikováno v:
Clinical Genetics. 53:293-297
We present an unusual case of monosomy 17p13-pter and monosomy Xp22.2-pter due to a dicentric translocation chromosome X/17 in a female newborn with severe anomalies. The karyotype was identified as 45,X,dic(X;17)(p22.2;p13) by high resolution GTG ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0780d73f22b94bc0c3c46fb10fdcb26b
https://doi.org/10.1111/j.1399-0004.1998.tb02699.x
https://doi.org/10.1111/j.1399-0004.1998.tb02699.x
Autor:
Wichard Vogel, Martin Steeg, Marius Horger, Peter Seizer, Sebastian P. Haen, Susanne Mackensen-Haen, Lothar Kanz, Michaela Rockenstiehl, Rebekka Mannal
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 141:634-634
Anamnese und klinischer Befund: Wir berichten uber einen 59-jahrigen Patienten mit akuten thorakalen Schmerzen. In der Vorgeschichte war eine Koronare Herzerkrankung bekannt. Der Patient berichtete weiterhin uber wechselnde Knochenschmerzen, seit ein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::238f1428458856dc048c23103423891b
https://doi.org/10.1055/s-0041-109909
https://doi.org/10.1055/s-0041-109909
Publikováno v:
The Journal of reproductive medicine. 52(10)
Clinically relevant acute twin-twin transfusion syndrome (TTTS) is a rare and poorly defined placental pathology because the definitions of chronic TTTS do not apply. Antepartum cases of acute TTTS are infrequently described in the literature despite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab98d2c4c6d49e57ca19233ce9f57f9b
https://pubmed.ncbi.nlm.nih.gov/17977173
https://pubmed.ncbi.nlm.nih.gov/17977173
Autor:
M. Meyer-Wittkopf, Rudi Beschorner, Michel Mittelbronn, Jens Schittenhelm, Benjamin Goeppert, David Capper, Richard Meyermann, Susanne Mackensen-Haen
Publikováno v:
Human pathology. 37(11)
Over the last 180 years, several theories concerning the origin of hydranencephaly have been proposed with an emphasis on infectious, aplastic, and vascular etiologies. In this report, we present a case of triplets with fetofetal transfusion syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a07c45ae2d51fb8b039ebaf32a454eae
https://pubmed.ncbi.nlm.nih.gov/16997352
https://pubmed.ncbi.nlm.nih.gov/16997352
Autor:
Diethelm Wallwiener, G. C. Meyberg-Solomayer, Susanne Mackensen-Haen, Tanja Fehm, E. F. Solomayer
Publikováno v:
Prenatal diagnosis. 24(10)
Objectives We report an atypical case of twin–twin transfusion syndrome (TTTS) in monochorionic-diamniotic twins with arterio-arterial anastomoses in which the former donor became the recipient during pregnancy. Methods Serial sonographic monitorin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c3b8c13effcdb8f068fcbd108f6d86e
https://pubmed.ncbi.nlm.nih.gov/15503278
https://pubmed.ncbi.nlm.nih.gov/15503278
Publikováno v:
American journal of perinatology. 14(2)
We describe a newborn infant with veno-occlusive disease (VOD) of the liver. Prior to discharge from the hospital, the newborn, who had been treated for suspected neonatal infection, suddenly developed sepsis-like symptoms. The size of the liver as w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::871ac0384a0e8dae927feeb63b24b55e
https://pubmed.ncbi.nlm.nih.gov/9259909
https://pubmed.ncbi.nlm.nih.gov/9259909
Autor:
Ulrike Orth, Andreas Dufke, Brigitte Vollmer, Heidemarie Kendziorra, Susanne Mackensen-Haen, Andreas Gal, Thorsten Orlikowsky
Publikováno v:
Karolinska Institutet
Careful investigation of hydrops fetalis (HF) is important with regard to genetic counselling and prenatal diagnosis. HF is known to be associated with various genetic disorders. To date there has been only one report of a male fetus in whom incontin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::363d9405304bcecfa810aa16307afb3a
http://www.ncbi.nlm.nih.gov/pubmed/11746157
http://www.ncbi.nlm.nih.gov/pubmed/11746157
