Zobrazeno 1 - 3
of 3
pro vyhledávání: '"S D Joustra"'
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0152390 (2016)
BACKGROUND:The suprachiasmatic nucleus (SCN) may play an important role in central autonomic control, since its projections connect to (para)sympathetic relay stations in the brainstem and spinal cord. The cardiac autonomic modifications during night
Externí odkaz:
https://doaj.org/article/c02eab2189824303ba53beedfdb3ad18
Autor:
J A Romijn, G J Lammers, R. van den Berg, N R Biermasz, S D Joustra, M. van Dijk, Roland D. Thijs, Alberto M. Pereira, E.J.W. van Someren
Publikováno v:
European Journal of Endocrinology, 171(2), 217-228. BioScientifica Ltd.
European Journal of Endocrinology, 171(2), 217-28. European Federation of Endocrine Societies
Joustra, S D, Thijs, R D, van de Berg, R, van Dijk, M, Pereira, A M, Lammers, G J, van Someren, E J W, Romijn, J A & Biermasz, N R 2014, ' Alterations in diurnal rhythmicity in patients treated for nonfunctioning pituitary macroadenoma: a controlled study and literature review ', European Journal of Endocrinology, vol. 171, no. 2, pp. 217-228 . https://doi.org/10.1530/EJE-14-0172
European Journal of Endocrinology, 171(2), 217-228
European Journal of Endocrinology, 171(2), 217-28. European Federation of Endocrine Societies
Joustra, S D, Thijs, R D, van de Berg, R, van Dijk, M, Pereira, A M, Lammers, G J, van Someren, E J W, Romijn, J A & Biermasz, N R 2014, ' Alterations in diurnal rhythmicity in patients treated for nonfunctioning pituitary macroadenoma: a controlled study and literature review ', European Journal of Endocrinology, vol. 171, no. 2, pp. 217-228 . https://doi.org/10.1530/EJE-14-0172
European Journal of Endocrinology, 171(2), 217-228
ObjectivePatients treated for nonfunctioning pituitary macroadenomas (NFMAs) have fatigue and alterations in sleep characteristics and sleep–wake rhythmicity frequently. As NFMAs often compress the optic chiasm, these complaints might be related to
Autor:
S D, Joustra, C A, Heinen, N, Schoenmakers, M, Bonomi, B E P B, Ballieux, M-O, Turgeon, D J, Bernard, E, Fliers, A S P, van Trotsenburg, M, Losekoot, L, Persani, J M, Wit, N R, Biermasz, A M, Pereira, W, Oostdijk, N, Zwaveling-Soonawala
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Mutations in the immunoglobulin superfamily, member 1 (IGSF1) gene cause the X-linked IGSF1 deficiency syndrome consisting of central hypothyroidism, delayed pubertal testosterone rise, adult macroorchidism, variable prolactin deficiency, and occasio