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.
242 related articles for article (PubMed ID: 25071871)
1. Developmental delay in Rett syndrome: data from the natural history study. Neul JL; Lane JB; Lee HS; Geerts S; Barrish JO; Annese F; Baggett LM; Barnes K; Skinner SA; Motil KJ; Glaze DG; Kaufmann WE; Percy AK J Neurodev Disord; 2014; 6(1):20. PubMed ID: 25071871 [TBL] [Abstract][Full Text] [Related]
2. Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis. Tarquinio DC; Hou W; Neul JL; Lane JB; Barnes KV; O'Leary HM; Bruck NM; Kaufmann WE; Motil KJ; Glaze DG; Skinner SA; Annese F; Baggett L; Barrish JO; Geerts SP; Percy AK Pediatr Neurol; 2015 Jun; 52(6):585-91.e2. PubMed ID: 25801175 [TBL] [Abstract][Full Text] [Related]
3. Distribution of hand function by age in individuals with Rett syndrome. Neul JL; Benke TA; Marsh ED; Lane JB; Lieberman DN; Skinner SA; Glaze DG; Suter B; Heydemann PT; Beisang AA; Standridge SM; Ryther RCC; Haas RH; Edwards LJ; Ananth A; Percy AK Ann Child Neurol Soc; 2023 Sep; 1(3):228-238. PubMed ID: 38496825 [TBL] [Abstract][Full Text] [Related]
4. [Mutation spectrum and genotype-phenotype correlation of MECP2 in patients with Rett syndrome]. Kondo I; Yamagata H No To Hattatsu; 2002 May; 34(3):219-23. PubMed ID: 12030010 [TBL] [Abstract][Full Text] [Related]
5. Multidimensional Development and Adaptive Behavioral Functioning in Younger and Older Children With Rett Syndrome. Wang SY; Lee WT; Shieh JY; Huang YH; Wong LC; Tsao CH; Chiu YL; Wu YT Phys Ther; 2022 Apr; 102(4):. PubMed ID: 35023562 [TBL] [Abstract][Full Text] [Related]
6. Characterizing the journey of Rett syndrome among females in the United States: a real-world evidence study using the Rett syndrome natural history study database. May D; Kponee-Shovein K; Neul JL; Percy AK; Mahendran M; Downes N; Chen G; Watson T; Pichard DC; Kennedy M; Lefebvre P J Neurodev Disord; 2024 Jul; 16(1):42. PubMed ID: 39061009 [TBL] [Abstract][Full Text] [Related]
7. Social impairments in Rett syndrome: characteristics and relationship with clinical severity. Kaufmann WE; Tierney E; Rohde CA; Suarez-Pedraza MC; Clarke MA; Salorio CF; Bibat G; Bukelis I; Naram D; Lanham DC; Naidu S J Intellect Disabil Res; 2012 Mar; 56(3):233-47. PubMed ID: 21385260 [TBL] [Abstract][Full Text] [Related]
8. Meaningful word acquisition is associated with walking ability over 10 years in Rett syndrome. Saikusa T; Kawaguchi M; Tanioka Tetsu T T; Nabatame Shin N S; Takahashi S; Yuge K; Nagamitsu SI; Takahashi T; Yamashita Y; Kobayashi Y; Hirayama C; Kakuma T; Matsuishi T; Itoh M Brain Dev; 2020 Nov; 42(10):705-712. PubMed ID: 32684376 [TBL] [Abstract][Full Text] [Related]
9. Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome. Inui K; Akagi M; Ono J; Tsukamoto H; Shimono K; Mano T; Imai K; Yamada M; Muramatsu T; Sakai N; Okada S Brain Dev; 2001 Jul; 23(4):212-5. PubMed ID: 11376998 [TBL] [Abstract][Full Text] [Related]
10. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. Cuddapah VA; Pillai RB; Shekar KV; Lane JB; Motil KJ; Skinner SA; Tarquinio DC; Glaze DG; McGwin G; Kaufmann WE; Percy AK; Neul JL; Olsen ML J Med Genet; 2014 Mar; 51(3):152-8. PubMed ID: 24399845 [TBL] [Abstract][Full Text] [Related]
11. Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients. Huppke P; Laccone F; Krämer N; Engel W; Hanefeld F Hum Mol Genet; 2000 May; 9(9):1369-75. PubMed ID: 10814718 [TBL] [Abstract][Full Text] [Related]
12. Epilepsy and the natural history of Rett syndrome. Glaze DG; Percy AK; Skinner S; Motil KJ; Neul JL; Barrish JO; Lane JB; Geerts SP; Annese F; Graham J; McNair L; Lee HS Neurology; 2010 Mar; 74(11):909-12. PubMed ID: 20231667 [TBL] [Abstract][Full Text] [Related]
13. MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning. Zahorakova D; Lelkova P; Gregor V; Magner M; Zeman J; Martasek P J Hum Genet; 2016 Jul; 61(7):617-25. PubMed ID: 26984561 [TBL] [Abstract][Full Text] [Related]
14. Growth failure and outcome in Rett syndrome: specific growth references. Tarquinio DC; Motil KJ; Hou W; Lee HS; Glaze DG; Skinner SA; Neul JL; Annese F; McNair L; Barrish JO; Geerts SP; Lane JB; Percy AK Neurology; 2012 Oct; 79(16):1653-61. PubMed ID: 23035069 [TBL] [Abstract][Full Text] [Related]
15. [MECP2 gene mutations in twenty-six cases with atypical Rett syndrome]. Li MR; Pan H; Bao XH; Zhang YZ; Jiang SL; Wu XR Zhonghua Er Ke Za Zhi; 2006 Apr; 44(4):285-8. PubMed ID: 16780651 [TBL] [Abstract][Full Text] [Related]
16. Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History Study. Neul JL; Benke TA; Marsh ED; Suter B; Silveira L; Fu C; Peters SU; Percy AK; Res Sq; 2023 Mar; ():. PubMed ID: 36993737 [TBL] [Abstract][Full Text] [Related]
17. Evaluation of QTc in Rett syndrome: Correlation with age, severity, and genotype. Crosson J; Srivastava S; Bibat GM; Gupta S; Kantipuly A; Smith-Hicks C; Myers SM; Sanyal A; Yenokyan G; Brenner J; Naidu SR Am J Med Genet A; 2017 Jun; 173(6):1495-1501. PubMed ID: 28394409 [TBL] [Abstract][Full Text] [Related]
18. Key clinical features to identify girls with CDKL5 mutations. Bahi-Buisson N; Nectoux J; Rosas-Vargas H; Milh M; Boddaert N; Girard B; Cances C; Ville D; Afenjar A; Rio M; Héron D; N'guyen Morel MA; Arzimanoglou A; Philippe C; Jonveaux P; Chelly J; Bienvenu T Brain; 2008 Oct; 131(Pt 10):2647-61. PubMed ID: 18790821 [TBL] [Abstract][Full Text] [Related]
19. Using Precision Medicine to Disentangle Genotype-Phenotype Relationships in Twins with Rett Syndrome: A Case Report. Singh J; Wilkins G; Goodman-Vincent E; Chishti S; Bonilla Guerrero R; Fiori F; Ameenpur S; McFadden L; Zahavi Z; Santosh P Curr Issues Mol Biol; 2024 Aug; 46(8):8424-8440. PubMed ID: 39194714 [TBL] [Abstract][Full Text] [Related]
20. Profiling scoliosis in Rett syndrome. Percy AK; Lee HS; Neul JL; Lane JB; Skinner SA; Geerts SP; Annese F; Graham J; McNair L; Motil KJ; Barrish JO; Glaze DG Pediatr Res; 2010 Apr; 67(4):435-9. PubMed ID: 20032810 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]