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Hyperprolinemia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hyperprolinemia" in English language version.

refsWebsite
Global rank English rank
14nih.gov
4th place
4th place
7doi.org
2nd place
2nd place
3worldcat.org
5th place
5th place
1web.archive.org
1st place
1st place
1semanticscholar.org
11th place
8th place

doi.org (Global: 2nd place; English: 2nd place)

  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. ISSN 1442-200X. PMC 4282441. PMID 24931297.
  • Jacquet, Hélène; Raux, Grégory; Thibaut, Florence; Hecketsweiler, Bernadette; Houy, Emmanuelle; Demilly, Caroline; Haouzir, Sadeq; Allio, Gabrielle; Fouldrin, Gael; Drouin, Valérie; Bou, Jacqueline; Petit, Michel; Campion, Dominique; Frébourg, Thierry (2002-09-15). "PRODH mutations and hyperprolinemia in a subset of schizophrenic patients". Human Molecular Genetics. 11 (19): 2243–2249. doi:10.1093/hmg/11.19.2243. ISSN 0964-6906. PMID 12217952.
  • Bender, Hans-Ulrich; Almashanu, Shlomo; Steel, Gary; Hu, Chien-An; Lin, Wei-Wen; Willis, Alecia; Pulver, Ann; Valle, David (March 2005). "Functional consequences of PRODH missense mutations". American Journal of Human Genetics. 76 (3): 409–420. doi:10.1086/428142. ISSN 0002-9297. PMC 1196393. PMID 15662599.
  • Harries, J. T.; Piesowicz, A. T.; Seakins, J. W. T.; Francis, D. E. M.; Wolff, O. H. (1 February 1971). "Low Proline Diet in Type 1 Hyperprolinaemia". Archives of Disease in Childhood. 46 (245): 72–81. doi:10.1136/adc.46.245.72. PMC 1647575. PMID 5555491.
  • Clelland, James D.; Read, Laura L.; Drouet, Valérie; Kaon, Angela; Kelly, Alexandra; Duff, Karen E.; Nadrich, Robert H.; Rajparia, Amit; Clelland, Catherine L. (June 2014). "Vitamin D insufficiency and schizophrenia risk: Evaluation of hyperprolinemia as a mediator of association". Schizophrenia Research. 156 (1): 15–22. doi:10.1016/j.schres.2014.03.017. PMC 4044915. PMID 24787057.
  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. PMC 4282441. PMID 24931297.
  • Bavaresco, CS; Streck, EL; Netto, CA; Wyse, AT (2005). "Chronic hyperprolinemia provokes a memory deficit in the Morris water maze task". Metab Brain Dis. 20 (1): 73–80. doi:10.1007/s11011-005-2478-x. PMID 15918552. S2CID 27367341.

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. ISSN 1442-200X. PMC 4282441. PMID 24931297.
  • Jacquet, Hélène; Raux, Grégory; Thibaut, Florence; Hecketsweiler, Bernadette; Houy, Emmanuelle; Demilly, Caroline; Haouzir, Sadeq; Allio, Gabrielle; Fouldrin, Gael; Drouin, Valérie; Bou, Jacqueline; Petit, Michel; Campion, Dominique; Frébourg, Thierry (2002-09-15). "PRODH mutations and hyperprolinemia in a subset of schizophrenic patients". Human Molecular Genetics. 11 (19): 2243–2249. doi:10.1093/hmg/11.19.2243. ISSN 0964-6906. PMID 12217952.
  • Bender, Hans-Ulrich; Almashanu, Shlomo; Steel, Gary; Hu, Chien-An; Lin, Wei-Wen; Willis, Alecia; Pulver, Ann; Valle, David (March 2005). "Functional consequences of PRODH missense mutations". American Journal of Human Genetics. 76 (3): 409–420. doi:10.1086/428142. ISSN 0002-9297. PMC 1196393. PMID 15662599.
  • Onenli-Mungan, N; Yüksel, B; Elkay, M; Topaloğlu, AK; et al. (2004). "Type II hyperprolinemia: A case study". The Turkish Journal of Pediatrics. 46 (2): 167–169. PMID 15214748.
  • Harries, J. T.; Piesowicz, A. T.; Seakins, J. W. T.; Francis, D. E. M.; Wolff, O. H. (1 February 1971). "Low Proline Diet in Type 1 Hyperprolinaemia". Archives of Disease in Childhood. 46 (245): 72–81. doi:10.1136/adc.46.245.72. PMC 1647575. PMID 5555491.
  • Clelland, James D.; Read, Laura L.; Drouet, Valérie; Kaon, Angela; Kelly, Alexandra; Duff, Karen E.; Nadrich, Robert H.; Rajparia, Amit; Clelland, Catherine L. (June 2014). "Vitamin D insufficiency and schizophrenia risk: Evaluation of hyperprolinemia as a mediator of association". Schizophrenia Research. 156 (1): 15–22. doi:10.1016/j.schres.2014.03.017. PMC 4044915. PMID 24787057.
  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. PMC 4282441. PMID 24931297.
  • Bavaresco, CS; Streck, EL; Netto, CA; Wyse, AT (2005). "Chronic hyperprolinemia provokes a memory deficit in the Morris water maze task". Metab Brain Dis. 20 (1): 73–80. doi:10.1007/s11011-005-2478-x. PMID 15918552. S2CID 27367341.

ncbi.nlm.nih.gov

  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. ISSN 1442-200X. PMC 4282441. PMID 24931297.
  • Bender, Hans-Ulrich; Almashanu, Shlomo; Steel, Gary; Hu, Chien-An; Lin, Wei-Wen; Willis, Alecia; Pulver, Ann; Valle, David (March 2005). "Functional consequences of PRODH missense mutations". American Journal of Human Genetics. 76 (3): 409–420. doi:10.1086/428142. ISSN 0002-9297. PMC 1196393. PMID 15662599.
  • Harries, J. T.; Piesowicz, A. T.; Seakins, J. W. T.; Francis, D. E. M.; Wolff, O. H. (1 February 1971). "Low Proline Diet in Type 1 Hyperprolinaemia". Archives of Disease in Childhood. 46 (245): 72–81. doi:10.1136/adc.46.245.72. PMC 1647575. PMID 5555491.
  • Clelland, James D.; Read, Laura L.; Drouet, Valérie; Kaon, Angela; Kelly, Alexandra; Duff, Karen E.; Nadrich, Robert H.; Rajparia, Amit; Clelland, Catherine L. (June 2014). "Vitamin D insufficiency and schizophrenia risk: Evaluation of hyperprolinemia as a mediator of association". Schizophrenia Research. 156 (1): 15–22. doi:10.1016/j.schres.2014.03.017. PMC 4044915. PMID 24787057.
  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. PMC 4282441. PMID 24931297.

ghr.nlm.nih.gov

semanticscholar.org (Global: 11th place; English: 8th place)

api.semanticscholar.org

web.archive.org (Global: 1st place; English: 1st place)

worldcat.org (Global: 5th place; English: 5th place)

search.worldcat.org

  • Mitsubuchi, Hiroshi; Nakamura, Kimitoshi; Matsumoto, Shirou; Endo, Fumio (August 2014). "Biochemical and clinical features of hereditary hyperprolinemia". Pediatrics International. 56 (4): 492–496. doi:10.1111/ped.12420. ISSN 1442-200X. PMC 4282441. PMID 24931297.
  • Jacquet, Hélène; Raux, Grégory; Thibaut, Florence; Hecketsweiler, Bernadette; Houy, Emmanuelle; Demilly, Caroline; Haouzir, Sadeq; Allio, Gabrielle; Fouldrin, Gael; Drouin, Valérie; Bou, Jacqueline; Petit, Michel; Campion, Dominique; Frébourg, Thierry (2002-09-15). "PRODH mutations and hyperprolinemia in a subset of schizophrenic patients". Human Molecular Genetics. 11 (19): 2243–2249. doi:10.1093/hmg/11.19.2243. ISSN 0964-6906. PMID 12217952.
  • Bender, Hans-Ulrich; Almashanu, Shlomo; Steel, Gary; Hu, Chien-An; Lin, Wei-Wen; Willis, Alecia; Pulver, Ann; Valle, David (March 2005). "Functional consequences of PRODH missense mutations". American Journal of Human Genetics. 76 (3): 409–420. doi:10.1086/428142. ISSN 0002-9297. PMC 1196393. PMID 15662599.