Zobrazeno 1 - 10
of 39
pro vyhledávání: '"H. P. H., Neumann"'
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p437-440, 4p
Autor:
E, von Dobschütz, H P H, Neumann
Publikováno v:
Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen. 90(1)
Chromaffin tumors, e.g. pheochromocytomas and paragangliomas are caused by germline mutations of several susceptibility genes in 30-40% of the patients. The corresponding syndromes are multiple endocrine neoplasia type 2 (MEN2, RET gene), von Hippel-
Autor:
A S, Hoekstra, B, van den Ende, X P, Julià, L, van Breemen, K, Scheurwater, C M, Tops, A, Malinoc, P, Devilee, H P H, Neumann, J-P, Bayley
Publikováno v:
Clinical genetics. 91(4)
Germline mutations in genes encoding subunits of succinate dehydrogenase (SDH) are associated with hereditary paraganglioma and pheochromocytoma. Although most mutations in SDHB, SDHC and SDHD are intraexonic variants, large germline deletions may re
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 111:350-354
Autor:
R. S. Kandt, H. P. H. Neumann
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 118:1577-1583
Autor:
H. P. H. Neumann, I. Zauner
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 118:25-29
Autor:
H P. H Neumann, Markus Cybulla
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 132:2271-2277
Fabry disease is an inherited X-linked lysosomal storage disease due to a genetic defect of the GLA gene which encodes the protein of the enzyme alpha-galaktosidase A. Under normal concentrations this lysosomal enzyme is involved in degradation and c
Publikováno v:
Der Nuklearmediziner. 30:70-82
In recent years, positron emission tomography with 6-[18F]fluoro-L-3,4-dihydroxyphenylalanine (FDOPA) has become a wide-spread method in the diagnostics of Parkinson's disease. The amino acid is an important component in protein metabolism. As a prec
Autor:
Wolfgang Maier, Carsten Christof Boedeker, Gerd Jürgen Ridder, H. P. H. Neumann, Joerg Schipper
Publikováno v:
Laryngo-Rhino-Otologie. 83:585-592
Background Paragangliomas of the head and neck represent rare tumors of neural crest origin that arise from chemoreceptors. They are highly vascular neoplasms that are benign in the majority of cases. There are controversial discussions concerning th
Publikováno v:
HNO. 52:651-662
Paragangliomas of the head and neck are preferably treated surgically. Planning the surgical approach for temporal bone paragangliomas is performed according to the Fisch classification. Small temporal paragangliomas can be removed in a transtympanic