Zobrazeno 1 - 10
of 16
pro vyhledávání: '"E M Ritzen"'
Autor:
Graziano Grugni, C. J. Partsch, A. L. Carrel, H. R. Mogul, M. Castro-Magana, Ora H. Pescovitz, C. Lammer, R. L. Hintz, R. G. Rosenfeld, Peter Davies, D. B. Allen, I. Sipila, Phillip D.K. Lee, Susan E. Myers, B. P. Hauffa, D. M. Wilson, E. M. Ritzen, Urs Eiholzer, M. A. Angulo, M. Cappa, G. Chiumello
Publikováno v:
The Endocrinologist. 10:71S-74S
Prader-Willi syndrome (PWS) is a disabling condition characterized by hypotonia, hyperphagia, obesity, short stature, delayed or absent puberty, and mental retardation. The syndrome complex was first described in 1956 by Dr. Andrea Prader and colleag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bcfe0b671fa70ef9dbe77a652bed5c0
https://doi.org/10.1097/00019616-200010041-00015
https://doi.org/10.1097/00019616-200010041-00015
Publikováno v:
Acta Paediatrica. 84:894-898
The pretreatment growth of 1 British and 14 Swedish children with late (2-7 years) diagnosis of 21-hydroxylase deficiency (210HD) was studied. The latter group included all patients diagnosed in Sweden after 1986. Twelve had mutations of the 21-hydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a03026798e752cd7eac8807a9ccc325d
https://doi.org/10.1111/j.1651-2227.1995.tb13788.x
https://doi.org/10.1111/j.1651-2227.1995.tb13788.x
Autor:
M, Parvinen, M, Kangasniemi, A, Kaipia, P, Mali, O, Soder, P, Pollanen, J, Toppari, I, Huhtaniemi, E M, Ritzen
Publikováno v:
Bulletin de l'Association des anatomistes. 75(228)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8e2fb4e352db537c71ff0ddcb6e61655
https://pubmed.ncbi.nlm.nih.gov/1664266
https://pubmed.ncbi.nlm.nih.gov/1664266
Publikováno v:
Acta Paediatrica. 85:761-761
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8732af6ccaa43a2b0c227f203a85e49c
https://doi.org/10.1111/j.1651-2227.1996.tb14145.x
https://doi.org/10.1111/j.1651-2227.1996.tb14145.x
Publikováno v:
Acta Endocrinologica. 77:S191-S198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e599365844a8ec592f9c66df0c66fa86
https://doi.org/10.1530/acta.0.077s191
https://doi.org/10.1530/acta.0.077s191
Publikováno v:
Europe PubMed Central
Soluble Mn2+-dependent adenylate cyclase and protein carboxyl methylase are two enzymes that are primarily localized in haploid germ cels of rat testicular tissue, and both enzymes exhibit an increase in activity in association with sexual maturation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::954c88b2af15dd8876ab514599601604
https://doi.org/10.1530/jrf.0.0770317
https://doi.org/10.1530/jrf.0.0770317
Autor:
E M Ritzen, G D Bloom
Publikováno v:
Zeitschrift f�r Zellforschung und Mikroskopische Anatomie. 61:841-854
Cells with autofluorescent granules are common in the dermal connective tissue of human skin. The cytoplasmic granules appear to be of lipo-pigment nature. The cells show phagocytic properties and it can therefore not be excluded that the cytoplasmic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4d1b63112e3febef0a6cac2d34556e
https://doi.org/10.1007/bf00340038
https://doi.org/10.1007/bf00340038
Autor:
P. Baggio, Antonia Mayerová, Laura Doria Lamba Carbone, J. Lindsten, A. Hjerpe, D. C. Rovetta, C. Sicchero, F. Lindgren, Ulrich Müller, E M Ritzen, M. Fraccaro, H. Ringertz, Ulrich Wolf, Franca Dagna Bricarelli
Publikováno v:
Human genetics. 57(1)
Three families with infants affected with campomelic dysplasia, a genetically determined mesenchymal disease frequently associated with sex reversal were studied. Two XY famales with ovarian gonadal differentiation and typical clinical features of ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d982add18004021ecc5bc480b257b288
https://pubmed.ncbi.nlm.nih.gov/7196380
https://pubmed.ncbi.nlm.nih.gov/7196380
Autor:
Finn P. Reinholt, E. M. Ritzen, Anders Hjerpe, Bo Wikström, Bengt Engfeldt, T. H. Bui, O. Eklöf
Publikováno v:
Acta paediatrica Scandinavica. 72(2)
The results of light and electron microscopic examination and of biochemical proteoglycan studies of costochondral and iliac crest biopsies from a recently diagnosed case of Dyggve-Melchior-Clausen dysplasia are reported. At light microscopy of resti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b37da0fc989780d3eab62f4a51331e36
https://pubmed.ncbi.nlm.nih.gov/6404126
https://pubmed.ncbi.nlm.nih.gov/6404126
Publikováno v:
Current topics in molecular endocrinology. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d0311c98845ac7ad778e49713df6209
https://pubmed.ncbi.nlm.nih.gov/141994
https://pubmed.ncbi.nlm.nih.gov/141994