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Correction: Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM.
Müller AR, Luijten MAJ, Haverman L, de Ranitz-Greven WL, Janssens P, Rietman AB, Hoopen LWT, de Graaff LCG, de Wit MC, Jansen AC, Gipson T, Capal JK, de Vries PJ, van Eeghen AM. Müller AR, et al. Among authors: van eeghen am. BMC Med. 2023 Oct 23;21(1):401. doi: 10.1186/s12916-023-03092-2. BMC Med. 2023. PMID: 37872559 Free PMC article. No abstract available.
Worries and needs of adults and parents of adults with neurofibromatosis type 1.
Rietman AB, van Helden H, Both PH, Taal W, Legerstee JS, van Staa A, Moll HA, Oostenbrink R, van Eeghen AM. Rietman AB, et al. Among authors: van helden h, van staa a, van eeghen am. Am J Med Genet A. 2018 May;176(5):1150-1160. doi: 10.1002/ajmg.a.38680. Am J Med Genet A. 2018. PMID: 29681082 Free PMC article.
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations.
Northrup H, Aronow ME, Bebin EM, Bissler J, Darling TN, de Vries PJ, Frost MD, Fuchs Z, Gosnell ES, Gupta N, Jansen AC, Jóźwiak S, Kingswood JC, Knilans TK, McCormack FX, Pounders A, Roberds SL, Rodriguez-Buritica DF, Roth J, Sampson JR, Sparagana S, Thiele EA, Weiner HL, Wheless JW, Towbin AJ, Krueger DA; International Tuberous Sclerosis Complex Consensus Group. Northrup H, et al. Pediatr Neurol. 2021 Oct;123:50-66. doi: 10.1016/j.pediatrneurol.2021.07.011. Epub 2021 Jul 24. Pediatr Neurol. 2021. PMID: 34399110 Free article.
Methylphenidate for attention-deficit/hyperactivity disorder in patients with Smith-Magenis syndrome: protocol for a series of N-of-1 trials.
Müller AR, Zinkstok JR, Rommelse NNJ, van de Ven PM, Roes KCB, Wijburg FA, de Rooij-Askes E, Linders C, Boot E, van Eeghen AM. Müller AR, et al. Among authors: van eeghen am, van de ven pm. Orphanet J Rare Dis. 2021 Sep 8;16(1):380. doi: 10.1186/s13023-021-02003-z. Orphanet J Rare Dis. 2021. PMID: 34496899 Free PMC article.
What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of 'Internal Medicine for Rare Genetic Syndromes'.
Rosenberg AGW, Pater MRA, Pellikaan K, Davidse K, Kattentidt-Mouravieva AA, Kersseboom R, Bos-Roubos AG, van Eeghen A, Veen JMC, van der Meulen JJ, van Aalst-van Wieringen N, Hoekstra FME, van der Lely AJ, de Graaff LCG. Rosenberg AGW, et al. J Clin Med. 2021 Nov 22;10(22):5457. doi: 10.3390/jcm10225457. J Clin Med. 2021. PMID: 34830739 Free PMC article.
The research landscape of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)-a comprehensive scoping review.
Vanclooster S, Bissell S, van Eeghen AM, Chambers N, De Waele L, Byars AW, Capal JK, Cukier S, Davis P, Flinn J, Gardner-Lubbe S, Gipson T, Heunis TM, Hook D, Kingswood JC, Krueger DA, Kumm AJ, Sahin M, Schoeters E, Smith C, Srivastava S, Takei M, Waltereit R, Jansen AC, de Vries PJ. Vanclooster S, et al. Among authors: van eeghen am. J Neurodev Disord. 2022 Feb 13;14(1):13. doi: 10.1186/s11689-022-09423-3. J Neurodev Disord. 2022. PMID: 35151277 Free PMC article. Review.
Empowering Families Through Technology: A Mobile-Health Project to Reduce the TAND Identification and Treatment Gap (TANDem).
Heunis TM, Bissell S, Byars AW, Capal JK, Chambers N, Cukier S, Davis PE, De Waele L, Flinn J, Gardner-Lubbe S, Gipson T, Kingswood JC, Krueger DA, Kumm AJ, Sahin M, Schoeters E, Smith C, Srivastava S, Takei M, Vanclooster S, van Eeghen AM, Waltereit R, Jansen AC, de Vries PJ. Heunis TM, et al. Among authors: van eeghen am. Front Psychiatry. 2022 Feb 28;13:834628. doi: 10.3389/fpsyt.2022.834628. eCollection 2022. Front Psychiatry. 2022. PMID: 35295772 Free PMC article.
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