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A message from holland.

BMJ (Clinical research ed.)

Thiadens HA.
PMID: 10856072
BMJ. 2000 Jun 17;320(7250):1655. doi: 10.1136/bmj.320.7250.1655.

No abstract available.

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Thiadens HA. A message from holland. BMJ. 2000;320(7250):1655doi: 10.1136/bmj.320.7250.1655.
Thiadens, H. A. (2000). A message from holland. BMJ (Clinical research ed.), 320(7250), 1655. https://doi.org/10.1136/bmj.320.7250.1655
Thiadens. "A message from holland." BMJ (Clinical research ed.) vol. 320,7250 (2000): 1655. doi: https://doi.org/10.1136/bmj.320.7250.1655
Thiadens HA. A message from holland. BMJ. 2000 Jun 17;320(7250):1655. doi: 10.1136/bmj.320.7250.1655. PMID: 10856072; PMCID: PMC1127430.
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Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry.

Acta ophthalmologica

Runhart EH, Dhooge P, Meester-Smoor M, Pas J, Pott JWR, van Leeuwen R, Kroes HY, Bergen AA, de Jong-Hesse Y, Thiadens AA, van Schooneveld MJ, van Genderen M, Boon C, Klaver C, van den Born LI, Cremers FPM, Hoyng CB.
PMID: 34431609
Acta Ophthalmol. 2021 Aug 25; doi: 10.1111/aos.14996. Epub 2021 Aug 25.

PURPOSE: To assess the incidence of Stargardt disease (STGD1) and to evaluate demographics of incident cases.METHODS: For this retrospective cohort study, demographic, clinical and genetic data of patients with a clinical diagnosis of STGD1 were registered between September 2010...

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Runhart EH, Dhooge P, Meester-Smoor M, et al. Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry. Acta Ophthalmol. 2021;doi: 10.1111/aos.14996.
Runhart, E. H., Dhooge, P., Meester-Smoor, M., Pas, J., Pott, J. W. R., van Leeuwen, R., Kroes, H. Y., Bergen, A. A., de Jong-Hesse, Y., Thiadens, A. A., van Schooneveld, M. J., van Genderen, M., Boon, C., Klaver, C., van den Born, L. I., Cremers, F. P. M., & Hoyng, C. B. (2021). Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry. Acta ophthalmologica, . https://doi.org/10.1111/aos.14996
Runhart, Esmee H, et al. "Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry." Acta ophthalmologica vol. (2021). doi: https://doi.org/10.1111/aos.14996
Runhart EH, Dhooge P, Meester-Smoor M, Pas J, Pott JWR, van Leeuwen R, Kroes HY, Bergen AA, de Jong-Hesse Y, Thiadens AA, van Schooneveld MJ, van Genderen M, Boon C, Klaver C, van den Born LI, Cremers FPM, Hoyng CB. Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry. Acta Ophthalmol. 2021 Aug 25; doi: 10.1111/aos.14996. Epub 2021 Aug 25. PMID: 34431609.
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Meiosis and sporulation induced in sporophytes of Ulva mutabilis ("slender") with synchronous mitosis.

Planta

Thiadens AJ, Zeuthen E.
PMID: 24554157
Planta. 1966 Mar;72(1):60-5. doi: 10.1007/BF00388145.

Sporulation preceded by meiosis was induced in young, diploid plants of Ulva mutabilis, mutant "slender" (FöYN). The induction was brought about either by replacement of the old culture medium (sea water plus soil extract) with new, or by the...

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Thiadens AJ, Zeuthen E. Meiosis and sporulation induced in sporophytes of Ulva mutabilis ("slender") with synchronous mitosis. Planta. 1966;72(1):60-5doi: 10.1007/BF00388145.
Thiadens, A. J., & Zeuthen, E. (1966). Meiosis and sporulation induced in sporophytes of Ulva mutabilis ("slender") with synchronous mitosis. Planta, 72(1), 60-5. https://doi.org/10.1007/BF00388145
Thiadens, A J, and Zeuthen, E. "Meiosis and sporulation induced in sporophytes of Ulva mutabilis ("slender") with synchronous mitosis." Planta vol. 72,1 (1966): 60-5. doi: https://doi.org/10.1007/BF00388145
Thiadens AJ, Zeuthen E. Meiosis and sporulation induced in sporophytes of Ulva mutabilis ("slender") with synchronous mitosis. Planta. 1966 Mar;72(1):60-5. doi: 10.1007/BF00388145. PMID: 24554157.
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Coronary artery fistulas.

Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation

Said SA, Thiadens AA, Fieren MJ, Meijboom EJ, van der Werf T, Bennink GB.
PMID: 25696067
Neth Heart J. 2002 Feb;10(2):65-78.

The aetiology of congenital coronary artery fistulas remains a challenging issue. Coronary arteries with an anatomically normal origin may, for obscure reasons, terminate abnormally and communicate with different single or multiple cardiac chambers or great vessels. When this occurs,...

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Said SA, Thiadens AA, Fieren MJ, et al. Coronary artery fistulas. Neth Heart J. 2002;10(2):65-78
Said, S. A., Thiadens, A. A., Fieren, M. J., Meijboom, E. J., van der Werf, T., & Bennink, G. B. (2002). Coronary artery fistulas. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation, 10(2), 65-78.
Said, S A M, et al. "Coronary artery fistulas." Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation vol. 10,2 (2002): 65-78.
Said SA, Thiadens AA, Fieren MJ, Meijboom EJ, van der Werf T, Bennink GB. Coronary artery fistulas. Neth Heart J. 2002 Feb;10(2):65-78. PMID: 25696067; PMCID: PMC2499687.
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X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients.

Ophthalmology

Hahn LC, van Schooneveld MJ, Wesseling NL, Florijn RJ, Ten Brink JB, Lissenberg-Witte BI, Strubbe I, Meester-Smoor MA, Thiadens AA, Diederen RM, van Cauwenbergh C, de Zaeytijd J, Walraedt S, de Baere E, Klaver CCW, Ossewaarde-van Norel J, Ingeborgh van den Born L, Hoyng CB, van Genderen MM, Sieving PA, Leroy BP, Bergen AA, Boon CJF.
PMID: 34624300
Ophthalmology. 2021 Oct 06; doi: 10.1016/j.ophtha.2021.09.021. Epub 2021 Oct 06.

PURPOSE: To describe the natural course, phenotype, and genotype of patients with X-linked retinoschisis (XLRS).DESIGN: Retrospective cohort study.PARTICIPANTS: Three hundred forty patients with XLRS from 178 presumably unrelated families.METHODS: This multicenter, retrospective cohort study reviewed medical records of patients...

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Hahn LC, van Schooneveld MJ, Wesseling NL, et al. X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients. Ophthalmology. 2021;doi: 10.1016/j.ophtha.2021.09.021.
Hahn, L. C., van Schooneveld, M. J., Wesseling, N. L., Florijn, R. J., Ten Brink, J. B., Lissenberg-Witte, B. I., Strubbe, I., Meester-Smoor, M. A., Thiadens, A. A., Diederen, R. M., van Cauwenbergh, C., de Zaeytijd, J., Walraedt, S., de Baere, E., Klaver, C. C. W., Ossewaarde-van Norel, J., Ingeborgh van den Born, L., Hoyng, C. B., van Genderen, M. M., Sieving, P. A., Leroy, B. P., Bergen, A. A., & Boon, C. J. F. (2021). X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients. Ophthalmology, . https://doi.org/10.1016/j.ophtha.2021.09.021
Hahn, Leo C, et al. "X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients." Ophthalmology vol. (2021). doi: https://doi.org/10.1016/j.ophtha.2021.09.021
Hahn LC, van Schooneveld MJ, Wesseling NL, Florijn RJ, Ten Brink JB, Lissenberg-Witte BI, Strubbe I, Meester-Smoor MA, Thiadens AA, Diederen RM, van Cauwenbergh C, de Zaeytijd J, Walraedt S, de Baere E, Klaver CCW, Ossewaarde-van Norel J, Ingeborgh van den Born L, Hoyng CB, van Genderen MM, Sieving PA, Leroy BP, Bergen AA, Boon CJF. X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients. Ophthalmology. 2021 Oct 06; doi: 10.1016/j.ophtha.2021.09.021. Epub 2021 Oct 06. PMID: 34624300.
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Showing 1 to 5 of 5 entries