Zobrazeno 1 - 10
of 81
pro vyhledávání: '"M. A. Spycher"'
Autor:
Antonio Rossi, M. A. Spycher, Georg Eich, Beat Steinmann, U. Stucki, P. Sacher, Andrea Superti-Furga
Publikováno v:
American Journal of Medical Genetics. 100:122-129
A boy presented at age 3.5 months with joint contractures, restlessness, and pain on handling. His skin was thickened and there were livid-red macular lesions over bony prominences. Infantile systemic hyalinosis (ISH) was diagnosed, a presumably auto
Autor:
Cecilia Giunta, Bernhard Zabel, M. A. Spycher, J. Briner, Georg Eich, Andrea Superti-Furga, Jörg Faber, Beat Steinmann, Andreas Winterpacht
Publikováno v:
Fetal and Pediatric Pathology. 18:187-206
Kniest dysplasia is a chondrodysplasia characterized by disproportionate dwarfism and facial dysmorphic features. Enchondral ossification of hyaline cartilage is impaired, and histologic examination of cartilage shows an abnormal structure (“Swiss
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 117:1014-1018
For 2 years a 72-year-old man had suffered from nonspecific upper abdominal discomfort and hepatomegaly. The gamma-glutamate transaminase concentration was increased to 121 U/l, the erythrocyte sedimentation rate was 80 mm in the first hour. Histolog
Publikováno v:
Scopus-Elsevier
SUMMARYPolyspecific IgG given intravenously at high doses (IVIG) is used for immunomodulatory therapy in autoimmune diseases such as idiopathic thrombocytopenic purpura and myasthenia gravis. It is assumed that the clinical effect is brought about in
Autor:
M. O. Spycher, P.J. Späth
Publikováno v:
Vox Sanguinis. 59:44-50
A sensitive flow-cytometric method was established to quantify the number of complement receptor 1 (CR1, C3b/C4b receptor, CD35) on the surface of purified erythrocytes of 12 patients infected by HIV-1 and showing two clinical AIDS-related complex/Wa
Publikováno v:
Transfusion medicine (Oxford, England). 14(2)
In this first-in-man study, we assessed the pharmacokinetics, safety and tolerability of MonoRho, a human recombinant monoclonal anti-RhD immunoglobulin G1 (IgG1) antibody. Eighteen RhD-negative healthy male volunteers were randomized in two groups t
Autor:
H, Walt, R, Hornung, D, Fink, D, Dobler-Girdziunaite, T, Stallmach, M A, Spycher, F, Maly, U, Haller, N, Bürki
Publikováno v:
Anticancer research. 21(5)
The aim of this study was to develop and characterize a mouse xenograft model for the hypercalcemic-type of small cell carcinoma of the ovary (HTSCCO).Tumor fragments were removed from a patient and cultured in six subsequent generations of nude mice
Autor:
M A Spycher, R. Gitzelmann
Publikováno v:
European Journal of Pediatrics. 152:592-594
Sediments prepared from freshly voided urine of four patients with glycogenosis Ia, or leucine-sensitive hypoglycaemia, on oral cornstarch therapy contained starch granules, evidence for persorption i.e. the incorporation of undissolved starch partic
Publikováno v:
American journal of medical genetics. 100(2)
A boy presented at age 3.5 months with joint contractures, restlessness, and pain on handling. His skin was thickened and there were livid-red macular lesions over bony prominences. Infantile systemic hyalinosis (ISH) was diagnosed, a presumably auto
Publikováno v:
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 52(1)
In 1956 Klingmüller first described the trichorhinophalangeal syndrome (TRPS), which was named by Giedion ten years later. The syndrome includes a combination of typical hair, facial and bone abnormalities with variable expression allowing the furth