Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Igor A. Harsch"'
Autor:
Igor Alexander Harsch
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Background. The Waterhouse–Friderichsen Syndrome (WFS) is a course of bacterial meningitis with a lethality rate that is still high today. One hallmark of the clinical course is intravascular coagulopathy. This causes hemorrhagic infarctions in the
Externí odkaz:
https://doaj.org/article/5e5fcee17dfd4973896d95745857a78a
Autor:
Igor Alexander Harsch
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 7, Iss 1, Pp 1-3 (2019)
Abstract Primary adrenal failure (Addison’s disease) is a rare complication of immune checkpoint inhibitor (ICI) therapy. Untreated – and also sometimes under adequate hydrocortisone replacement therapy – the levels of ACTH (Adrenocorticotropic
Externí odkaz:
https://doaj.org/article/51c66e3ba93f491aa8d9120dc912f0bd
Autor:
Igor Alexander Harsch
Publikováno v:
Clinical Case Reports, Vol 8, Iss 7, Pp 1315-1316 (2020)
Abstract Abdominal erythema ab igne may be the result of insufficient pain medication in chronic pancreatitis. Stenting therapy is to be considered, and the patient should be informed about the risk of developing cutaneous squamous or Merkel cell car
Externí odkaz:
https://doaj.org/article/a2f55e41848c4b2ca5f71499142bf48f
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2019 (2019)
Fecal microbiota transplantation (FMT) is a novel strategy for the therapy of dysbiosis-associated disorders via modulation of the gut microbiota. Intestinal dysbiosis is associated not only with digestive disorders, but also with a variety of extra-
Externí odkaz:
https://doaj.org/article/ee674088b9744b8ea4237cad794880b5
Autor:
Igor Alexander Harsch
Publikováno v:
Clinical Case Reports, Vol 7, Iss 12, Pp 2598-2599 (2019)
Abstract In patients who had no medical care for years, it is wise to expect the unexpected. Here, a gigantic liver cyst compressed abdominal organs, vessels, and the gut. The patient is thus far doing well in a nursing home, exemplifying the low amo
Externí odkaz:
https://doaj.org/article/f5df24f08900428b8166266a2395f119
Publikováno v:
Clinical Case Reports, Vol 7, Iss 11, Pp 2269-2270 (2019)
Abstract Pheochromocytoma is a rare reason for hypertension. At least in younger people, an endocrinological workup of the etiology of hypertension is mandatory, as this case describes. If the pheochromocytomas are large enough, they can not only lea
Externí odkaz:
https://doaj.org/article/9faf24a9172b43bab4ae6ac52e546a7d
Autor:
Igor Alexander Harsch
Publikováno v:
Clinical Case Reports, Vol 7, Iss 9, Pp 1813-1814 (2019)
Abstract Lipohypertrophies frequently occur during insulin therapy. They alter insulin absorption, causing higher insulin requirements (and costs), fluctuating blood glucose and episodes of unpredictable hypoglycemia. Screening is mandatory, as well
Externí odkaz:
https://doaj.org/article/29f7761f62c94bc882a3bcd31bb0919a
Autor:
Peter Christopher Konturek, Igor Alexander Harsch, Kathrin Konturek, Monic Schink, Thomas Konturek, Markus F. Neurath, Yurdaguel Zopf
Publikováno v:
Medical Sciences, Vol 6, Iss 3, p 79 (2018)
Chronic liver diseases are a major cause of morbidity and mortality worldwide. Recently, gut dysbiosis was identified as an important factor in the pathogenesis of liver diseases. The relationship between gut microbiota and the liver is still not wel
Externí odkaz:
https://doaj.org/article/35b01612b2844bbeaf3665908468d589
Publikováno v:
Medical Sciences, Vol 6, Iss 2, p 32 (2018)
The investigation of the human microbiome is the most rapidly expanding field in biomedicine. Early studies were undertaken to better understand the role of microbiota in carbohydrate digestion and utilization. These processes include polysaccharide
Externí odkaz:
https://doaj.org/article/820ac8686d63452a9052dd78c750613d
Publikováno v:
Wiadomości Lekarskie. 72:124-128
Turner syndrome can be manifest with a considerable genetic and phenotypic variability. This merely accounts for about 50% of patients who do not have the “classic” 45 X genotype. We report the case of a 42-year-old female patient with a 46, X, d