These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
262 related items for PubMed ID: 25934608
1. [Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]. Poisson A, Nicolas A, Sanlaville D, Cochat P, De Leersnyder H, Rigard C, Franco P, des Portes V, Edery P, Demily C. Arch Pediatr; 2015 Jun; 22(6):638-45. PubMed ID: 25934608 [Abstract] [Full Text] [Related]
2. Behavioral disturbance and treatment strategies in Smith-Magenis syndrome. Poisson A, Nicolas A, Cochat P, Sanlaville D, Rigard C, de Leersnyder H, Franco P, Des Portes V, Edery P, Demily C. Orphanet J Rare Dis; 2015 Sep 04; 10():111. PubMed ID: 26336863 [Abstract] [Full Text] [Related]
3. Smith-Magenis syndrome. De Leersnyder H. Handb Clin Neurol; 2013 Sep 04; 111():295-6. PubMed ID: 23622179 [Abstract] [Full Text] [Related]
4. Smith-Magenis syndrome and its circadian influence on development, behavior, and obesity - own experience. Chen L, Mullegama SV, Alaimo JT, Elsea SH. Dev Period Med; 2015 Sep 04; 19(2):149-56. PubMed ID: 26384114 [Abstract] [Full Text] [Related]
5. [Diagnostic difficulties in Smith-Magenis Syndrome (SMS) on the basis of own experience and literature data]. Stembalska A, Jakubiak A, Śmigiel R. Med Wieku Rozwoj; 2012 Sep 04; 16(2):138-43. PubMed ID: 22971658 [Abstract] [Full Text] [Related]
6. Twenty-four-hour motor activity and body temperature patterns suggest altered central circadian timekeeping in Smith-Magenis syndrome, a neurodevelopmental disorder. Smith ACM, Morse RS, Introne W, Duncan WC. Am J Med Genet A; 2019 Feb 04; 179(2):224-236. PubMed ID: 30690916 [Abstract] [Full Text] [Related]
7. [Inversion of the circadian melatonin rhythm in Smith-Magenis syndrome]. De Leersnyder H, de Blois MC, Bresson JL, Sidi D, Claustrat B, Munnich A. Rev Neurol (Paris); 2003 Nov 04; 159(11 Suppl):6S21-6. PubMed ID: 14646795 [Abstract] [Full Text] [Related]
8. Circadian rhythm disorder in a rare disease: Smith-Magenis syndrome. De Leersnyder H, Claustrat B, Munnich A, Verloes A. Mol Cell Endocrinol; 2006 Jun 27; 252(1-2):88-91. PubMed ID: 16723183 [Abstract] [Full Text] [Related]
9. Inverted rhythm of melatonin secretion in Smith-Magenis syndrome: from symptoms to treatment. De Leersnyder H. Trends Endocrinol Metab; 2006 Sep 27; 17(7):291-8. PubMed ID: 16890450 [Abstract] [Full Text] [Related]
10. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Smith ACM, Boyd KE, Brennan C, Charles J, Elsea SH, Finucane BM, Foster R, Gropman A, Girirajan S, Haas-Givler B. ; 1993 Sep 27. PubMed ID: 20301487 [Abstract] [Full Text] [Related]
11. Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2). Gropman AL, Duncan WC, Smith AC. Pediatr Neurol; 2006 May 27; 34(5):337-50. PubMed ID: 16647992 [Abstract] [Full Text] [Related]
12. [Sleep disturbance associated with Smith-Magenis syndrome]. Pan M, Chen L. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec 10; 38(12):1262-1265. PubMed ID: 34839521 [Abstract] [Full Text] [Related]
13. A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome. Tug E, Cine N, Aydin H. Genet Couns; 2011 Dec 10; 22(1):11-9. PubMed ID: 21614983 [Abstract] [Full Text] [Related]
14. Management of Sleep Disturbances Associated with Smith-Magenis Syndrome. Kaplan KA, Elsea SH, Potocki L. CNS Drugs; 2020 Jul 10; 34(7):723-730. PubMed ID: 32495322 [Abstract] [Full Text] [Related]
15. First Case Report of Smith-Magenis Syndrome (SMS) Among the Arab Community in Nazareth: View and Overview. Nijim Y, Adawi A, Bisharat B, Bowirrat A. Medicine (Baltimore); 2016 Jan 10; 95(3):e2362. PubMed ID: 26817868 [Abstract] [Full Text] [Related]
16. Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder. Poisson A, Nicolas A, Bousquet I, Raverot V, Gronfier C, Demily C. Int J Mol Sci; 2019 Jul 19; 20(14):. PubMed ID: 31330985 [Abstract] [Full Text] [Related]
17. First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutation. Acquaviva F, Sana ME, Della Monica M, Pinelli M, Postorivo D, Fontana P, Falco MT, Nardone AM, Lonardo F, Iascone M, Scarano G. Am J Med Genet A; 2017 Jan 19; 173(1):231-238. PubMed ID: 27683195 [Abstract] [Full Text] [Related]
18. Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity. Williams SR, Zies D, Mullegama SV, Grotewiel MS, Elsea SH. Am J Hum Genet; 2012 Jun 08; 90(6):941-9. PubMed ID: 22578325 [Abstract] [Full Text] [Related]
19. Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome. De Leersnyder H, De Blois MC, Claustrat B, Romana S, Albrecht U, Von Kleist-Retzow JC, Delobel B, Viot G, Lyonnet S, Vekemans M, Munnich A. J Pediatr; 2001 Jul 08; 139(1):111-6. PubMed ID: 11445803 [Abstract] [Full Text] [Related]
20. Phase advance of circadian rhythms in Smith-Magenis syndrome: a case study in an adult man. Kocher L, Brun J, Devillard F, Azabou E, Claustrat B. Neurosci Lett; 2015 Jan 12; 585():144-8. PubMed ID: 25434872 [Abstract] [Full Text] [Related] Page: [Next] [New Search]