Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Vera van Tellingen"'
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Akademický článek
The Hyponatremic Hypertensive Syndrome in a Preterm Infant: A Case of Severe Hyponatremia with Neurological Sequels
Autor: Vera van Tellingen, Marc R. Lilien, Jos F. M. Bruinenberg, Willem B. de Vries
Publikováno v: International Journal of Nephrology, Vol 2011 (2011)
Objective. To report the irreversible severe neurological symptoms following the hyponatremic hypertensive syndrome (HHS) in an infant after umbilical arterial catheterization. Design. Case report with review of the literature. Setting. Neonatal inte
Externí odkaz: https://doaj.org/article/2f47c796833345b983f856edd7b73743
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2
Optimizing the timing of highest hydrocortisone dose in children and adolescents with 21-hydroxylase deficiency
Autor: Antonius E. van Herwaarden, Gianni Bocca, Sabine E. Hannema, Dina A. Schott, Erica L T van den Akker, Paul N. Span, Hedi L Claahsen-van der Grinten, Hetty J. van der Kamp, Fred C.G.J. Sweep, Janiëlle A E M van der Velden, Christiaan F. Mooij, Mariska A M Schröder, Saartje Straetemans, Sandra W.K. de Kort, Vera van Tellingen
Publikováno v: Schroder, M A M, van Herwaarden, A E, Span, P N, van den Akker, E L T, Bocca, G, Hannema, S E, van der Kamp, H J, de Kort, S W K, Mooij, C F, Schott, D A, Straetemans, S, Van Tellingen, V, van der Velden, J A, Sweep, F C G J & Grinten, H L C D 2021, ' Optimizing the timing of highest hydrocortisone dose in children and adolescents with 21-hydroxylase deficiency ', Hormone Research in Paediatrics, vol. 94, no. SUPPL 1, pp. 63-64 .
Hormone Research in Paediatrics, 94(SUPPL 1), 63-64. S. Karger AG
Journal of Clinical Endocrinology and Metabolism, 107(4), E1661-E1672. The Endocrine Society
Schröder, M A M, Van Herwaarden, A E, Span, P N, Van Den Akker, E L T, Bocca, G, Hannema, S E, Van Der Kamp, H J, De Kort, S W K, Mooij, C F, Schott, D A, Straetemans, S, Van Tellingen, V, Van Der Velden, J A, Sweep, F C G J & Claahsen-Van Der Grinten, H L 2022, ' Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency ', Journal of Clinical Endocrinology and Metabolism, vol. 107, no. 4, pp. E1661-E1672 . https://doi.org/10.1210/clinem/dgab826
Journal of Clinical Endocrinology and Metabolism, 107, E1661-E1672
Journal of Clinical Endocrinology and Metabolism, 107, 4, pp. E1661-E1672
Schröder, M A M, van Herwaarden, A E, Span, P N, van den Akker, E L T, Bocca, G, Hannema, S E, van der Kamp, H J, de Kort, S W K, Mooij, C F, Schott, D A, Straetemans, S, van Tellingen, V, van der Velden, J A, Sweep, F C G J & van der Grinten, H L C 2021, ' Optimizing the timing of highest hydrocortisone dose in children and adolescents with 21-hydroxylase deficiency ', The Journal of clinical endocrinology and metabolism . https://doi.org/10.1210/clinem/dgab826
The Journal of clinical endocrinology and metabolism. The Endocrine Society
Journal of clinical endocrinology and metabolism, 107(4), E1661-E1672. The Endocrine Society
Journal of Clinical Endocrinology & Metabolism, 107(4), E1661-E1672. ENDOCRINE SOC
Journal of Clinical Endocrinology & Metabolism, 107(4), E1661-E1672. Oxford University Press
Journal of Clinical Endocrinology and Metabolism, 107(4), E1661-E1672. Endocrine Society
Context Hydrocortisone treatment of young patients with 21-hydroxylase deficiency (21OHD) is given thrice daily, but there is debate about the optimal timing of the highest hydrocortisone dose, either mimicking the physiological diurnal rhythm (morni
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6cade1ce4b17d153caec8b6b27afbce
https://research.vumc.nl/en/publications/8ffc5d4b-b9b2-4d48-be26-611f54a31d24
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3
Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study
Autor: Kevin Stroek, Henk Engel, Marelle J. Bouva, Sabine E. Hannema, Anita Boelen, Mirjam E. van Albada, Annemieke C. Heijboer, Evelien A Kemper, Gianni Bocca, Hedi L Claahsen-van der Grinten, E. C. A. Mieke Houdijk, Mariëtte T. Ackermans, An F. C. Ruiter, A S Paul van Trotsenburg, Vera van Tellingen, Hetty J. van der Kamp, Annelieke A A van der Linde, Erica L T van den Akker, Robert de Jonge, Nitash Zwaveling-Soonawala, Bernadette S. Jakobs, Annet M. Bosch, Martijn J J Finken
Publikováno v: The Journal of clinical endocrinology and metabolism, 106(11), E4487-E4496. The Endocrine Society
Journal of clinical endocrinology and metabolism, 106(11), E4487-E4496. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 106, e4487-e4496
Stroek, K, Ruiter, A, van der Linde, A, Ackermans, M, Bouva, M J, Engel, H, Jakobs, B, Kemper, E A, van den Akker, E L T, van Albada, M E, Bocca, G, Finken, M J J, Hannema, S E, Mieke Houdijk, E C A, van der Kamp, H J, van Tellingen, V, Paul van Trotsenburg, A S, Zwaveling-Soonawala, N, Bosch, A M, de Jonge, R, Heijboer, A C, Claahsen-van der Grinten, H L & Boelen, A 2021, ' Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands : A Newborn Screening Pilot Study ', The Journal of clinical endocrinology and metabolism, vol. 106, no. 11, pp. E4487-E4496 . https://doi.org/10.1210/clinem/dgab464
Journal of Clinical Endocrinology and Metabolism, 106(11), e4487-e4996. ENDOCRINE SOC
Journal of Clinical Endocrinology and Metabolism, 106(11), E4487-E4496. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 106, 11, pp. e4487-e4496
Context Newborn screening (NBS) for classic congenital adrenal hyperplasia (CAH) consists of 17-hydroxyprogesterone (17-OHP) measurement with gestational age–adjusted cutoffs. A second heel puncture (HP) is performed in newborns with inconclusive r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ee7993770982c91f946003f91c388e
https://pubmed.ncbi.nlm.nih.gov/34171085
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4
Age-Specific Reference Intervals for Plasma Free Thyroxine and Thyrotropin in Term Neonates During the First Two Weeks of Life
Autor: A S Paul van Trotsenburg, Charlotte A Heinen, Eric Fliers, Nitash Zwaveling-Soonawala, Sophie R.D. Van Der Schoor, Annemieke C. Heijboer, Vera van Tellingen, Jolanda C. Naafs, Anita Boelen
Publikováno v: Thyroid, 30(8), 1106-1111. Mary Ann Liebert Inc.
Naafs, J C, Heinen, C A, Zwaveling-Soonawala, N, Van Der Schoor, S R D, Van Tellingen, V, Heijboer, A C, Fliers, E, Boelen, A & Van Trotsenburg, A S P 2020, ' Age-specific reference intervals for plasma free thyroxine and thyrotropin in term neonates during the first two weeks of life ', Thyroid, vol. 30, no. 8, pp. 1106-1111 . https://doi.org/10.1089/thy.2019.0779
Background: Congenital hypothyroidism (CH) is a common and preventable cause of mental retardation, which is detected in many neonatal screening programs. Upon suspicion of CH, plasma free thyroxine (fT4) and thyrotropin (TSH) concentrations are meas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c0a8f09c1cac21d0c69172f8e8a2a4
https://pubmed.ncbi.nlm.nih.gov/32126889
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5
Long-term follow-up after bilateral percutaneous epiphysiodesis around the knee to reduce excessive predicted final height
Autor: Arnold T Besselaar, Willie M. Bakker-van Waarde, R. J. Odink, Frank Jonkers, Florens Q. M. P. van Douveren, Marieke C. van der Steen, Annemieke Boot, Wesley J Goedegebuure, Minne Heeg, Vera van Tellingen
Publikováno v: Archives of Disease in Childhood, 103(3), 219-223. BMJ PUBLISHING GROUP
ContextPercutaneous epiphysiodesis (PE) around the knee to reduce predicted excessive final height. Studies until now included small numbers of patients and short follow-up periods.Objective and designThis Dutch multicentre, long-term, retrospective,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f759e24319aff7b157aed2f314654a0
https://research.rug.nl/en/publications/54163f7a-51b3-41ed-a5b6-c220f5b2eaec
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6
The Hyponatremic Hypertensive Syndrome in a Preterm Infant: A Case of Severe Hyponatremia with Neurological Sequels
Autor: Marc R. Lilien, Jos F. M. Bruinenberg, Willem B. de Vries, Vera van Tellingen
Publikováno v: International Journal of Nephrology, Vol 2011 (2011)
International Journal of Nephrology
Objective. To report the irreversible severe neurological symptoms following the hyponatremic hypertensive syndrome (HHS) in an infant after umbilical arterial catheterization. Design. Case report with review of the literature. Setting. Neonatal inte
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12f00a57d5b2c0e06fc2208736482a9
https://doi.org/10.4061/2011/406515
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7
Inverted fixation-off sensitivity in atypical benign partial epilepsy
Autor: Vivianne van Kranen-Mastenbroek, Joost Nicolai, Johan S.H. Vles, Vera van Tellingen
Publikováno v: Pediatric neurology. 38(4)
Fixation-off sensitivity is an electroencephalographic phenomenon characterized by spike-and-wave discharges that only occur when central vision and fixation are eliminated. It is especially seen in children with Panayiotopoulos-type, early-onset, be
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ef2c2043a003d4192ecf3554fd9fb9d
https://pubmed.ncbi.nlm.nih.gov/18358409
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8
Akademický článek
MRI Diagnosis of Occipital Cephalohematoma Mimicking an Encephalocele.
Autor: Vera van Tellingen
Publikováno v: American Journal of Perinatology; Feb2008, Vol. 25 Issue 3, p153-155, 3p
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