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For: Kuhlmann L, Joensson IM, Froekjaer JB, Krogh K, Farholt S. A descriptive study of colorectal function in adults with Prader-Willi Syndrome: high prevalence of constipation. BMC Gastroenterol 2014;14:63. [PMID: 24708524 DOI: 10.1186/1471-230X-14-63] [Cited by in Crossref: 16] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Passone CBG, Pasqualucci PL, Franco RR, Ito SS, Mattar LBF, Koiffmann CP, Soster LA, Carneiro JDA, Cabral Menezes-Filho H, Damiani D. PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW. Rev Paul Pediatr 2018;36:345-52. [PMID: 30365815 DOI: 10.1590/1984-0462/;2018;36;3;00003] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
2 Salehi P, Lee D, Ambartsumyan L, Sikka N, Scheimann AO. Rectal Picking Masquerading as Inflammatory Bowel Disease in Prader-Willi Syndrome: . Journal of Pediatric Gastroenterology and Nutrition 2018;67:59-63. [DOI: 10.1097/mpg.0000000000001937] [Cited by in Crossref: 3] [Article Influence: 0.8] [Reference Citation Analysis]
3 Salles J, Lacassagne E, Benvegnu G, Berthoumieu SÇ, Franchitto N, Tauber M. The RDoC approach for translational psychiatry: Could a genetic disorder with psychiatric symptoms help fill the matrix? the example of Prader-Willi syndrome. Transl Psychiatry 2020;10:274. [PMID: 32772048 DOI: 10.1038/s41398-020-00964-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
4 Smith L, Berkowitz MR. Osteopathic approach to chronic constipation in Prader–Willi Syndrome: A case report. International Journal of Osteopathic Medicine 2016;19:73-7. [DOI: 10.1016/j.ijosm.2015.11.002] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]
5 Butler MG. Prolapsed Rectum and Risk Factors in Prader-Willi Syndrome: A Case-Based Review. J Pediatr Genet 2022;11:1-4. [PMID: 35186383 DOI: 10.1055/s-0041-1724049] [Reference Citation Analysis]
6 Pellikaan K, van Woerden GM, Kleinendorst L, Rosenberg AGW, Horsthemke B, Grosser C, van Zutven LJCM, van Rossum EFC, van der Lely AJ, Resnick JL, Brüggenwirth HT, van Haelst MM, de Graaff LCG. The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature. Genes (Basel) 2021;12:875. [PMID: 34200226 DOI: 10.3390/genes12060875] [Reference Citation Analysis]
7 Kanclerz P. Accommodative insufficiency in a patient with Prader-Willi syndrome and SNRPN gene mutation. Saudi J Ophthalmol 2020;34:56-8. [PMID: 33542990 DOI: 10.4103/1319-4534.301291] [Reference Citation Analysis]
8 Alyousif Z, Miller JL, Sandoval MY, MacPherson CW, Nagulesapillai V, Dahl WJ. The effects of Bifidobacterium animalis ssp. lactis B94 on gastrointestinal wellness in adults with Prader-Willi syndrome: study protocol for a randomized controlled trial. Trials 2018;19:256. [PMID: 29703235 DOI: 10.1186/s13063-018-2648-x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
9 Robertson J, Baines S, Emerson E, Hatton C. Prevalence of constipation in people with intellectual disability: A systematic review. Journal of Intellectual & Developmental Disability 2017;43:392-406. [DOI: 10.3109/13668250.2017.1310829] [Cited by in Crossref: 10] [Article Influence: 2.0] [Reference Citation Analysis]
10 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. 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'. J Clin Med 2021;10:5457. [PMID: 34830739 DOI: 10.3390/jcm10225457] [Reference Citation Analysis]
11 Alyousif Z, Miller JL, Auger J, Sandoval M, Piano A, Tompkins TA, Dahl WJ. Microbiota profile and efficacy of probiotic supplementation on laxation in adults affected by Prader-Willi Syndrome: A randomized, double-blind, crossover trial. Mol Genet Genomic Med 2020;8:e1535. [PMID: 33103385 DOI: 10.1002/mgg3.1535] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Pellikaan K, Snijders F, Rosenberg AGW, Davidse K, van den Berg SAA, Visser WE, van der Lely AJ, de Graaff LCG. Thyroid Function in Adults with Prader-Willi Syndrome; a Cohort Study and Literature Review. J Clin Med 2021;10:3804. [PMID: 34501256 DOI: 10.3390/jcm10173804] [Reference Citation Analysis]
13 McCarthy J, Lupo PJ, Kovar E, Rech M, Bostwick B, Scott D, Kraft K, Roscioli T, Charrow J, Schrier Vergano SA, Lose E, Smiegel R, Lacassie Y, Schaaf CP. Schaaf-Yang syndrome overview: Report of 78 individuals. Am J Med Genet A 2018;176:2564-74. [PMID: 30302899 DOI: 10.1002/ajmg.a.40650] [Cited by in Crossref: 32] [Cited by in F6Publishing: 29] [Article Influence: 8.0] [Reference Citation Analysis]
14 Dahl WJ, Auger J, Alyousif Z, Miller JL, Tompkins TA. Adults with Prader-Willi syndrome exhibit a unique microbiota profile. BMC Res Notes 2021;14:51. [PMID: 33549146 DOI: 10.1186/s13104-021-05470-6] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]