Zobrazeno 1 - 10
of 202
pro vyhledávání: '"Pfäffle, R."'
Publikováno v:
Drug Design, Development and Therapy, Vol Volume 11, Pp 1489-1495 (2017)
Juan Pedro López-Siguero,1 Roland Pfäffle,2 Philippe Chanson,3 Mieczyslaw Szalecki,4,5 Nadja Höbel,6 Markus Zabransky6 1Servicio de Endocrinología Pediátrica, Hospital Materno-Infantil, Hospital Regional Universitario de Málaga, Spain; 2Univers
Externí odkaz:
https://doaj.org/article/4eee6ae43fde4e6a935e621e713ab20e
Publikováno v:
RöFo: Fortschritte auf dem Gebiet der Röntgenstrahlen und der Bildgebenden Verfahren; 2024 Supplement 2, Vol. 196, pS132-S133, 2p
The second 360° European Meeting on Growth Hormone Disorders, held in Barcelona, Spain, in June 2017, included a session entitled Pragmatism vs. Curiosity in Genetic Diagnosis of Growth Disorders, which examined current concepts of genetics and grow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::91fbb1d2c26d3d9385ecb04be1518e55
https://openaccess.sgul.ac.uk/id/eprint/111268/1/fendo-10-00602.pdf
https://openaccess.sgul.ac.uk/id/eprint/111268/1/fendo-10-00602.pdf
Publikováno v:
62. Jahrestagung der Deutschen Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie e.V. (GMDS); 20170917-20170921; Oldenburg; DOCAbstr. 191 /20170829/
Introduction: Abnormal growth is a cardinal symptom. There are many disorders, which cause aberrant growth. This makes it hard to find out all correct diagnoses in early years of childhood development. To support primary care pediatricians in their d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8f1f1a16fc02d209455ae9bf858650a
Publikováno v:
Pituitary. 5:163-168
Combined pituitary hormone deficiency (CPHD) can be caused by mutation of the pituitary transcription factors POU1F1 or PROP1. More recently mutations in the HESX1, the LHX3 and LHX4 transcription factor genes have also been described as a cause in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fe946d139df3f10da0c3baf441a68e9
https://doi.org/10.1023/a:1023356915458
https://doi.org/10.1023/a:1023356915458
Autor:
Hermanussen, M., Meitinger, T., Veldhuis, J. D., Low, M. J., Pfäffle, R., Staub, K., Panczak, R., Groth, D., Brabec, M., Von Salisch, M., Loh, C. P.A., Tassenaar, V., Scheffler, C., Mumm, R., Godina, E., Lehmann, A., Tutkuviene, J., Gervickaite, S., Nierop, A. F.M., Holmgren, A., Aßmann, C., Van Buuren, S., Koziel, S., Zadzińska, E., Varela-Silva, I., Vignerová, J., Salama, E., El-Shabrawi, M., Huijic, A., Satake, T., Bogin, B.
Publikováno v:
Hermanussen, M, Meitinger, T, Veldhuis, J D, Low, M J, Pfäffle, R, Staub, K, Panczak, R, Groth, D, Brabec, M, Von Salisch, M, Loh, C P A, Tassenaar, V, Scheffler, C, Mumm, R, Godina, E, Lehmann, A, Tutkuviene, J, Gervickaite, S, Nierop, A F M, Holmgren, A, Aßmann, C, Van Buuren, S, Koziel, S, Zadzińska, E, Varela-Silva, I, Vignerová, J, Salama, E, El-Shabrawi, M, Huijic, A, Satake, T & Bogin, B 2014, ' Adolescent growth : Genes, hormones and the peer group. Proceedings of the 20th aschauer Soiree, held at Glücksburg Castle, Germany, 15th to 17th November 2013 ', Pediatric Endocrinology Reviews, vol. 11, no. 3, pp. 341-353 .
The association between poverty, malnutrition, illness and poor socioeconomic conditions on the one side, and poor growth and short adult stature on the other side, is well recognized. Yet, the simple assumption by implication that poor growth and sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3697::986b7e752182d47ce93c79f852362319
http://www.scopus.com/inward/record.url?scp=84899577524&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=84899577524&partnerID=8YFLogxK
Autor:
Hoppmann, J., Vasilakis, I., Vogel, M., Stoll, S., Gesing, J., Gausche, R., Kratzsch, J., Körner, A., Pfäffle, R., Kiess, W.
Publikováno v:
Kinder- und Jugendmedizin; April 2019, Vol. 19 Issue: 2 p80-90, 11p
Autor:
Kiess, W., Gesing, J., Körner, A., Sergeyev, E., Merkenschlager, A., Kapellen, T., Pfäffle, R.
Publikováno v:
Kinder- und Jugendmedizin; February 2019, Vol. 19 Issue: 1 p9-17, 9p
Autor:
Ahmet Caglayan, Klammt, J., Kiess, W., Hatipoglu, N., Pfäffle, R., Kurtoglu, S., Saatci, C., Dundar, M.
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Publons
Munis Dundar
Europe PubMed Central
Publons
Munis Dundar
A unique case of a patient with partial trisomy 22 and lipodystrophy: is it a new syndrome due to an IGF-IR mutation?: A newborn male presented with intestinal malrotation, facial anomalies, hypertrichosis, hypertrophic, hyperpigmented nipples and en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::48e088cc488ba8c44f18f15ae31c68ef
https://avesis.deu.edu.tr/publication/details/03c0b6d3-428e-4174-b487-a1c1ee87e54b/oai
https://avesis.deu.edu.tr/publication/details/03c0b6d3-428e-4174-b487-a1c1ee87e54b/oai
Publikováno v:
European Journal of Pediatrics. 1997, Vol. 156 Issue 11, p835. 3p.