Zobrazeno 1 - 10
of 121
pro vyhledávání: '"H. Neering"'
Autor:
Belinda Reinhardt, Sarah H. Neering, Astrid Klocke, Ulrike Peters, Thomas Frank Flemmig, Thomas Beikler, Sabine Selbach
Publikováno v:
Clinical oral investigations. 23(10)
Suppression of periodontal pathogens in the oral cavity of periodontally healthy individuals may lower the risk for periodontal or periimplant diseases. Therefore, the present study aimed to analyze the effect of supragingival debridement (SD) with a
Autor:
Thomas Frank Flemmig, Astrid Klocke, Sabine Adyani-Fard, Thomas Beikler, Stefan Rüttermann, Sarah H. Neering
Publikováno v:
BMC Oral Health
BACKGROUND: Plasminogen deficiency is a rare autosomal recessive disease, which is associated with aggressive periodontitis and gingival enlargement. Previously described treatments of plasminogen deficiency associated periodontitis have shown limite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f909cde8f0f716229e626234d0c9dba4
http://publikationen.ub.uni-frankfurt.de/files/40528/12903-015-0045-3.pdf
http://publikationen.ub.uni-frankfurt.de/files/40528/12903-015-0045-3.pdf
Autor:
Thijn R Brummelkamp, Annette M.G. Dirac, René Bernards, H. Neering, Sebastian M.B. Nijman, W.J. Mooi, HM Oosterkamp
Publikováno v:
British Journal of Dermatology. 155:182-185
Summary Background Familial cylindromatosis is a rare genetic disorder, giving rise to neoplasms of the skin appendages. We have recently shown that loss of the cylindromatosis tumour suppressor gene leads to activation of NF-jB, a transcription fact
Publikováno v:
European journal of surgical oncology, 29(1), 81-86. W.B. Saunders Ltd
Aims: To investigate the results of our treatment policy, we present our institutional experience in the management of regional neck node metastases of cutaneous head and neck squamous cell carcinoma (CHNSCC). Methods: Between 1977 and 1997, 343 pati
Autor:
H M, Oosterkamp, H, Neering, S M B, Nijman, A M G, Dirac, W J, Mooi, R, Bernards, T R, Brummelkamp
Publikováno v:
The British journal of dermatology. 155(1)
Familial cylindromatosis is a rare genetic disorder, giving rise to neoplasms of the skin appendages. We have recently shown that loss of the cylindromatosis tumour suppressor gene leads to activation of NF-kappaB, a transcription factor having antia
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 143(39)
Publikováno v:
The Lancet. 336:464-466
16 patients with recurrent staphylococcal furunculosis but without anaemia had significantly lower serum iron concentrations than normal laboratory reference values, 8 controls with single furuncles, or 10 controls with acne conglobata. There were no
Autor:
H. Neering
Publikováno v:
British Journal of Dermatology. 93:229-230
Publikováno v:
Cancer. 72(8)
Two cases of malignant melanoma associated with neurofibromatosis in two first-degree female relatives from a family with familial atypical multiple mole melanoma (FAMMM) syndrome are presented. The types of neurofibromatosis and the FAMMM syndrome a
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 137(32)