Menonita (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Menonita" in Galician language version.

refsWebsite
Global rank Galician rank
4th place
6th place
4,380th place
1,519th place
222nd place
134th place
low place
low place
low place
low place
low place
1,890th place
9,919th place
low place

amazon.es

  • Dyck CJ. (1993). An introduction to Mennonite history: A popular history of the Anabaptists and the Mennonites. Scottdale, PA: Herald Press. p 452. [4]

neurology.org

n.neurology.org

  • Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC. (2005). A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia. Neurology 65:156–158. [14]

nih.gov

ncbi.nlm.nih.gov

  • Wilson RC, Dave-Sharma S, Wei JQ, Obeyesekere VR, Li K, Ferrari P, Krozowski ZS, Shackleton CH, Bradlow L, Wiens T, NewMI. 1998. A genetic defect resulting in mild low-renin hypertension. Proc Natl Acad Sci USA 95:10200–10205. PMID 9707624 . DOI: 10.1073/pnas.95.17.10200
  • Ugrasbul F, Wiens T, Rubinstein P, New MI & Wilson RC.. 1999. Prevalence of mild apparent mineralocorticoid excess in Mennonites. Journal of Clinical Endocrinology and Metabolism 84 4735–4738 . DOI: 10.1210/jcem.84.12.6340 . PMID 10599743 .
  • Campbell C, Mitui M, Eng L, Coutinho G, Thorstenson Y, Gatti RA. (2003). ATM mutations on distinct SNP and STR haplotypes in ataxia-telangiectasia patients of differing ethnicities reveal ancestral founder effects. Hum Mutat 21:80–85. PMID 12497634 . DOI: 10.1002/humu.10156 .
  • Mitui M, Bernatowska E, Pietrucha B, Piotrowska-Jastrzebska J, Eng L, Nahas S, Teraoka S, Sholty G, Purayidom A, Concannon P, Gatti RA. (2005). ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia. Ann Hum Genet 69:657–664. PMID 16266405 . DOI: 10.1111/j.1529-8817.2005.00199.x
  • Kagimoto M, Winter JS, Kagimoto K, Simpson ER, Waterman MR. (1988). Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: Molecular basis of one example of combined 17 alpha-hydroxylase/17, 20 lyase deficiency. Mol Endocrinol 2:564–570. PMID 2843762 . DOI: 10.1210/mend-2-6-564
  • Imai T, Yanase T, Waterman MR, Simpson ER, Pratt JJ. (1992). Canadian Mennonites and individuals residing in the Friesland region of The Netherlands share the same molecular basis of 17 alpha-hydroxylase deficiency. Hum Genet 89: 95–96. DOI: 10.1007/bf00207050 . PMID 1577471
  • Greenberg CR, Evans JA, McKendry-Smith S, Redekopp S, Haworth JC, Mulivor R, Chodirker BN. (1990). Infantile hypophosphatasia: Localization within chromosome region 1p36. 1-34 and prenatal diagnosis using linked DNA markers. Am J Hum Genet 46:286–292. PMID 1689104 . PMCID: PMC1684978
  • Greenberg CR, Taylor CL, Haworth JC, Seargeant LE, Philipps S, Triggs-Raine B, Chodirker BN. (1993). A homoallelic Gly317— >Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian Mennonites. Genomics 17:215–217. PMID 8406453 . DOI: 10.1006/geno.1993.1305
  • Arpaia E, Shahar M, Dadi H, Cohen A, Roifman CM. (1994). Defective T cell receptor signaling and CD8þthymic selection in humans lacking zap-70 kinase. Cell 76:947–958. doi: 10.1016/0092-8674(94)90368-9. PMID 8124727 . [5]
  • Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE. (1998). Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 338:1248–1257. doi: 10.1056/NEJM199804303381802. PMID 9562578 . [6]
  • Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, Litt M. (1994). Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KC NA1. Nat Genet 8:136–140. doi: 10.1038/ng1094-136. PMID 7842011 . [10]
  • Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA. (1996). Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias. Arch Neurol 53:338–344. doi: 10.1001/archneur.1996.00550040074016. PMID 8929156 . [11]
  • Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR. (1996). Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1 A4. Cell 87:543–552. doi: 10.1016/s0092-8674(00)81373-2. PMID 8898206 . [12]
  • Steckley JL, Ebers GC, Cader MZ, McLachlan RS. (2001). An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. Neurology 57:1499–1502. doi: 10.1212/wnl.57.8.1499. PMID 11673600 . [13]
  • Braybrook C, Doudney K, Marcano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P. (2001). The Tbox transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia. Nat Genet 29:179–183. doi: 10.1038/ng730 . PMID 11559848 . [15]
  • Renpenning H, Gerrard JW, Zaleski WA, Tabata T. (1962). Familial sex-linked mental retardation. Can Med Assoc J 87:954–956. PMID 13981686 . [16]
  • Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE. (1998). Renpenning syndrome maps to Xp11. Am J Hum Genet 62:1092–1101. doi: 10.1086/301835. PMID 9545405 . [17]

pubmed.ncbi.nlm.nih.gov

  • Arpaia E, Shahar M, Dadi H, Cohen A, Roifman CM. (1994). Defective T cell receptor signaling and CD8þthymic selection in humans lacking zap-70 kinase. Cell 76:947–958. doi: 10.1016/0092-8674(94)90368-9. PMID 8124727 . [5]
  • Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE. (1998). Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 338:1248–1257. doi: 10.1056/NEJM199804303381802. PMID 9562578 . [6]
  • Alders M, Jongbloed R, Deelen W, van den Wijngaard A, Doevendans P, Ten Cate F, Regitz-Zagrosek V, Vosberg HP, van Langen I, Wilde A, Dooijes D, Mannens M. (2003). The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands. Eur Heart J 24:1848–1853. doi: 10.1016/s0195-668x(03)00466-4. [7]
  • McManus K, Lupe K, Coghlan G, Zelinski T. (2000). An amino acid substitution in the putative second extracellular loop of RBC band 3 accounts for the Froese blood group polymorphism. Transfusion 40:1246–1249. doi: 10.1046/j.1537-2995.2000.40101246.x. [8]
  • Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, Litt M. (1994). Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KC NA1. Nat Genet 8:136–140. doi: 10.1038/ng1094-136. PMID 7842011 . [10]
  • Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA. (1996). Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias. Arch Neurol 53:338–344. doi: 10.1001/archneur.1996.00550040074016. PMID 8929156 . [11]
  • Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR. (1996). Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1 A4. Cell 87:543–552. doi: 10.1016/s0092-8674(00)81373-2. PMID 8898206 . [12]
  • Steckley JL, Ebers GC, Cader MZ, McLachlan RS. (2001). An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. Neurology 57:1499–1502. doi: 10.1212/wnl.57.8.1499. PMID 11673600 . [13]
  • Braybrook C, Doudney K, Marcano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P. (2001). The Tbox transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia. Nat Genet 29:179–183. doi: 10.1038/ng730 . PMID 11559848 . [15]
  • Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE. (1998). Renpenning syndrome maps to Xp11. Am J Hum Genet 62:1092–1101. doi: 10.1086/301835. PMID 9545405 . [17]

omim.org

sinauer.com

  • Hartl DL, Clark AG. 1997. Principles of Population Genetics. 3rd editon. Sunderland, MA: Sinauer Associates. p 542. [2]

wiley.com

onlinelibrary.wiley.com

  • Connolly MB, Jan JE, Couch RM, Wong LT, Dimmick JE, Rigg JM. 1991. Hepatic dysfunction in Alstrom disease. AmJ Med Genet 40:421–424. [3]
  • Zelinski T, McKeown I, McAlpine PJ, Philipps S, Coghlan G. (1996). Assignment of the gene(s) governing Froese and Swann blood group polymorphism to chromosome 17q. Transfusion 36: 419–420. [9]

wwu.edu

cedar.wwu.edu

  • Martin, K, J. C. Stevenson, M. H. Crawford et al. 1996. Immunoglobin haplotype frequencies in Anabaptist population samples: Kansas and Nebraska Mennonites and Indiana Amish. Hum. Biol. 68:45-62. [1]