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Zespół Pradera-Williego (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół Pradera-Williego" in Polish language version.

refsWebsite
Global rank Polish rank
40nih.gov
4th place
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24doi.org
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1emedicine.com
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1endojournals.org
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1aappublications.org
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1okiem-stasia-b.blogspot.com
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1tvn.pl
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aappublications.org

pediatrics.aappublications.org

doi.org

dx.doi.org

doi.org

  • de Lind van Wijngaarden RF., de Klerk LW., Festen DA., Duivenvoorden HJ., Otten BJ., Hokken-Koelega AC. Randomized controlled trial to investigate the effects of growth hormone treatment on scoliosis in children with Prader-Willi syndrome.. „The Journal of clinical endocrinology and metabolism”. 4 (94), s. 1274–80, kwiecień 2009. DOI: 10.1210/jc.2008-1844. PMID: 19158197. 
  • Kobayashi J, Kodama M, Yamazaki K, Morikawa O, Murano S, Kawamata N, Kawamura I. Gastric Bypass in a Japanese Man with Prader-Willi Syndrome and Morbid Obesity. „Obesity Surgery”. 13. 5, 2003. DOI: 10.1381/096089203322509453. PMID: 14627483. 
  • Couper RT, Couper JJ. Prader-Willi syndrome. „Lancet”. 356. 9230, s. 673-5, 2000. DOI: 10.1016/S0140-6736(00)02617-9. PMID: 10968453. 

emedicine.com

endojournals.org

edrv.endojournals.org

nih.gov

ncbi.nlm.nih.gov

  • M.G. Butler, Prader-Willi syndrome: current understanding of cause and diagnosis, „American Journal of Medical Genetics”, 35 (3), 1990, s. 319–332, DOI: 10.1002/ajmg.1320350306, PMID: 2309779, PMCID: PMC5493042.
  • O.C. Ward, Prader-Willi syndrome, „The Lancet”, 356 (9244), 2000, s. 1856, DOI: 10.1016/S0140-6736(05)73324-9, PMID: 11117944.
  • O.C. Ward, Down's 1864 case of Prader-Willi syndrome: a follow-up report, „Journal of the Royal Society of Medicine”, 90 (12), 1997, s. 694–696, DOI: 10.1177/014107689709001221, PMID: 9496304, PMCID: PMC1296748.
  • H.J. Schneider, H. Zellweger, Forme fruste of the Prader-Willi syndrome (HHHO) and balanced D-E translocation, „Helvetica Paediatrica Acta”, 23 (2), 1968, s. 128–135, PMID: 4387003.
  • D.H. Ledbetter i inni, Deletions of chromosome 15 as a cause of the Prader-Willi syndrome, „The New England Journal of Medicine”, 304 (6), 1981, s. 325–329, DOI: 10.1056/NEJM198102053040604, PMID: 7442771.
  • M.G. Butler, C.G. Palmer, Parental origin of chromosome 15 deletion in Prader-Willi syndrome, „The Lancet”, 1 (8336), 1983, s. 1285–1286, DOI: 10.1016/S0140-6736(83)92745-9, PMID: 6134086, PMCID: PMC5510872.
  • R.D. Nicholls i inni, Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome, „Nature”, 342 (6247), 1989, s. 281–285, DOI: 10.1038/342281a0, PMID: 2812027.
  • L. Hudgins, J.S. Geer, S.B. Cassidy, Phenotypic differerencss in African Americans with Prader-Willi syndrome, „Genetics in Medicine”, 1 (1), 1998, s. 49–51, DOI: 10.1097/00125817-199811000-00010, PMID: 11261430.
  • H. Ehara, K. Ohno, K. Takeshita, Frequency of the Prader-Willi syndrome in the San-in district, Japan, „Brain & Development”, 17 (5), 1995, s. 324–326, DOI: 10.1016/0387-7604(95)00060-O, PMID: 8579217.
  • Eve Oiglane-Shlik i inni, Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented, „American Journal of Medical Genetics. Part A”, 140 (18), 2006, s. 1936–1943, DOI: 10.1002/ajmg.a.31423, PMID: 16906556.
  • Annick Vogels i inni, Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders, „European journal of human genetics: EJHG”, 12 (3), 2004, s. 238–240, DOI: 10.1038/sj.ejhg.5201135, PMID: 14679397.
  • A. Smith i inni, Birth prevalence of Prader-Willi syndrome in Australia, „Archives of Disease in Childhood”, 88 (3), 2003, s. 263–264, DOI: 10.1136/adc.88.3.263, PMID: 12598399, PMCID: PMC1719461.
  • J.E. Whittington i inni, Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region, „Journal of Medical Genetics”, 38 (11), 2001, s. 792–798, DOI: 10.1136/jmg.38.11.792, PMID: 11732491, PMCID: PMC1734766.
  • Douglas C. Bittel, Merlin G. Butler, Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology, „Expert Reviews in Molecular Medicine”, 7 (14), 2005, s. 1–20, DOI: 10.1017/S1462399405009531, PMID: 16038620.
  • Sara Rodriguez-Jato i inni, Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus, „Nucleic Acids Research”, 33 (15), 2005, s. 4740–4753, DOI: 10.1093/nar/gki786, PMID: 16116039, PMCID: PMC1188517.
  • Boris V. Skryabin i inni, Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation, „PLoS genetics”, 3 (12), 2007, e235, DOI: 10.1371/journal.pgen.0030235, PMID: 18166085, PMCID: PMC2323313.
  • T. Yang i inni, A mouse model for Prader-Willi syndrome imprinting-centre mutations, „Nature Genetics”, 19 (1), 1998, s. 25–31, DOI: 10.1038/ng0598-25, PMID: 9590284.
  • S.M. Strakowski, M.G. Butler, Paternal hydrocarbon exposure in Prader-Willi syndrome, „The Lancet”, 2 (8573), 1987, s. 1458, DOI: 10.1016/S0140-6736(87)91152-4, PMID: 2892013.
  • S.B. Cassidy, A.J. Gainey, M.G. Butler, Occupational hydrocarbon exposure among fathers of Prader-Willi syndrome patients with and without deletions of 15q, „American Journal of Human Genetics”, 44 (6), 1989, s. 806–810, PMID: 2729276, PMCID: PMC1715664.
  • Birgitt Schüle i inni, Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome, „BMC medical genetics”, 6, 2005, s. 18, DOI: 10.1186/1471-2350-6-18, PMID: 15877813, PMCID: PMC1142316.
  • C.R. Hamilton, R.E. Scully, B. Kliman, Hypogonadotropinism in Prader-Willi syndrome. Induction of puberty and sperm altogenesis by clomiphene citrate, „The American Journal of Medicine”, 52 (3), 1972, s. 322–329, PMID: 5011391.
  • A. Crinò i inni, Hypogonadism and pubertal development in Prader-Willi syndrome, „European Journal of Pediatrics”, 162 (5), 2003, s. 327–333, DOI: 10.1007/s00431-002-1132-4, PMID: 12692714.
  • A.C. Lindgren i inni, Eating behavior in Prader-Willi syndrome, normal weight, and obese control groups, „The Journal of Pediatrics”, 137 (1), 2000, s. 50–55, DOI: 10.1067/mpd.2000.106563, PMID: 10891821.
  • D.J. Aughton, S.B. Cassidy, Physical features of Prader-Willi syndrome in neonates, „American Journal of Diseases of Children”, 144 (11), 1990, s. 1251–1254, DOI: 10.1001/archpedi.1990.02150350083032, PMID: 2239867.
  • R.W. Hered i inni, Ophthalmologic features of Prader-Willi syndrome, „Journal of Pediatric Ophthalmology and Strabismus”, 25 (3), 1988, s. 145–150, PMID: 3397859.
  • G.A. Scardina, G. Fucà, P. Messina, Oral diseases in a patient affected with Prader-Willi syndrome, „European Journal of Paediatric Dentistry”, 8 (2), 2007, s. 96–99, PMID: 17571934.
  • Bhargava SA, Putnam PE, Kocoshis SA, Rowe M, Hanchett JM. Rectal bleeding in Prader-Willi syndrome. „Pediatrics”. 97, s. 265-267, 1996. PMID: 8584392. 
  • Dykens EM. Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?. „J Child Psychol Psychiatry”. 43. 3, s. 343-52, 2002. PMID: 11944876. 
  • Burman P, Ritzén EM, Lindgren AC. Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH. „Endocr Rev”. 22. 6, s. 787-99, 2001. PMID: 11739333. 
  • Wharton RH, Wang T, Graeme-Cook F, Briggs S, Cole RE. Acute idiopathic gastric dilation with gastric necrosis in individuals with Prader-Willi syndrome. „Am J Med Genet”. 73, s. 437-41, 1997. PMID: 9415471. 
  • Stevenson DA, Heinemann J, Angulo M, Butler MG, Loker J, Rupe N, Kendell P, Cassidy SB, Scheimann A. Gastric rupture and necrosis in Prader-Willi syndrome. „J Pediatr Gastroenterol Nutr”. 45(. 2, s. 272-4, 2007. PMID: 17667731. 
  • Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F. Prader-Willi syndrome: consensus diagnostic criteria. „Pediatrics”. 91. 2, s. 398-402, 1993. PMID: 8424017. 
  • Gunay-Aygun M, Schwartz S, Heeger S, O’Riordan MA, Cassidy SB. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. „Pediatrics”. 108. 5, s. E92, 2001. PMID: 11694676. 
  • de Lind van Wijngaarden RF., de Klerk LW., Festen DA., Duivenvoorden HJ., Otten BJ., Hokken-Koelega AC. Randomized controlled trial to investigate the effects of growth hormone treatment on scoliosis in children with Prader-Willi syndrome.. „The Journal of clinical endocrinology and metabolism”. 4 (94), s. 1274–80, kwiecień 2009. DOI: 10.1210/jc.2008-1844. PMID: 19158197. 
  • Kobayashi J, Kodama M, Yamazaki K, Morikawa O, Murano S, Kawamata N, Kawamura I. Gastric Bypass in a Japanese Man with Prader-Willi Syndrome and Morbid Obesity. „Obesity Surgery”. 13. 5, 2003. DOI: 10.1381/096089203322509453. PMID: 14627483. 
  • Scheimann AO, Butler MG, Gourash L, Cuffari C, Klish W. Critical analysis of bariatric procedures in Prader-Willi syndrome. „J Pediatr Gastroenterol Nutr”. 46. 1, s. 80-3, 2008. PMID: 18162838. 
  • Couper RT, Couper JJ. Prader-Willi syndrome. „Lancet”. 356. 9230, s. 673-5, 2000. DOI: 10.1016/S0140-6736(00)02617-9. PMID: 10968453. 
  • Carpenter PK. Prader-Willi syndrome in old age. „J Intellect Disabil Res”. 38. Pt 5, s. 529-531, 1994. PMID: 7841690. 
  • Butler MG. A 68-year-old white female with Prader-Willi syndrome. „Clin Dysmorphol”. 9, s. 65-67, 2000. PMID: 10649803. 
  • Pozzilli P, Khazrai YM. „La Monstrua Vestida”. a case of Prader-Willi syndrome. „J Endocrinol Invest”. 28. 2, s. 199, 2005. PMID: 15887871. 

okiem-stasia-b.blogspot.com

  • Okiem Stasia B [online], okiem-stasia-b.blogspot.com [dostęp 2017-11-28].

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