אהרן חנוקוגלו (Hebrew Wikipedia)

Analysis of information sources in references of the Wikipedia article "אהרן חנוקוגלו" in Hebrew language version.

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doi.org

  • Hanukoglu A (1991). "Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects". J Clin Endocrinol Metab. 73 (5): 936–44. doi:10.1210/jcem-73-5-936. PMID 1939532.
  • Strautnieks SS, Thompson RJ, Hanukoglu A, Dillon MJ, Hanukoglu I, Kuhnle U (1996). "Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping". Hum Mol Genet. 5 (2): 293–9. doi:10.1093/hmg/5.2.293. PMID 8824886.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Chang SS, Grunder S, Hanukoglu A, Rösler A, Mathew PM, Hanukoglu I (1996). "Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1". Nat Genet. 12 (3): 248–53. doi:10.1038/ng0396-248. PMID 8589714.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Saxena A, Hanukoglu I, Saxena D, Thompson RJ, Gardiner RM, Hanukoglu A (2002). "Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genes". J Clin Endocrinol Metab. 87 (7): 3344–50. doi:10.1210/jcem.87.7.8674. PMID 12107247.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Edelheit O, Hanukoglu I, Gizewska M, Kandemir N, Tenenbaum-Rakover Y, Yurdakök M; et al. (2005). "Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism". Clin Endocrinol (Oxf). 62 (5): 547–53. doi:10.1111/j.1365-2265.2005.02255.x. PMID 15853823.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Hanukoglu A, Edelheit O, Shriki Y, Gizewska M, Dascal N, Hanukoglu I (2008). "Renin-aldosterone response, urinary Na/K ratio and growth in pseudohypoaldosteronism patients with mutations in epithelial sodium channel (ENaC) subunit genes". J Steroid Biochem Mol Biol. 111 (3–5): 268–74. doi:10.1016/j.jsbmb.2008.06.013. PMID 18634878.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Hanukoglu I, Hanukoglu A (2016). "Epithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseases". Gene. 579 (2): 95–132. doi:10.1016/j.gene.2015.12.061. PMC 4756657. PMID 26772908.
  • Hanukoglu A, Vargas-Poussou R, Landau Z, Yosovich K, Hureaux M, Zennaro MC (2020). "Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 gene". J Steroid Biochem Mol Biol. 204: 105755. doi:10.1016/j.jsbmb.2020.105755. PMID 33017655.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Hanukoglu A (1991). "Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects". J Clin Endocrinol Metab. 73 (5): 936–44. doi:10.1210/jcem-73-5-936. PMID 1939532.
  • Strautnieks SS, Thompson RJ, Hanukoglu A, Dillon MJ, Hanukoglu I, Kuhnle U (1996). "Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping". Hum Mol Genet. 5 (2): 293–9. doi:10.1093/hmg/5.2.293. PMID 8824886.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Chang SS, Grunder S, Hanukoglu A, Rösler A, Mathew PM, Hanukoglu I (1996). "Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1". Nat Genet. 12 (3): 248–53. doi:10.1038/ng0396-248. PMID 8589714.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Saxena A, Hanukoglu I, Saxena D, Thompson RJ, Gardiner RM, Hanukoglu A (2002). "Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genes". J Clin Endocrinol Metab. 87 (7): 3344–50. doi:10.1210/jcem.87.7.8674. PMID 12107247.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Edelheit O, Hanukoglu I, Gizewska M, Kandemir N, Tenenbaum-Rakover Y, Yurdakök M; et al. (2005). "Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism". Clin Endocrinol (Oxf). 62 (5): 547–53. doi:10.1111/j.1365-2265.2005.02255.x. PMID 15853823.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Hanukoglu A, Edelheit O, Shriki Y, Gizewska M, Dascal N, Hanukoglu I (2008). "Renin-aldosterone response, urinary Na/K ratio and growth in pseudohypoaldosteronism patients with mutations in epithelial sodium channel (ENaC) subunit genes". J Steroid Biochem Mol Biol. 111 (3–5): 268–74. doi:10.1016/j.jsbmb.2008.06.013. PMID 18634878.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
  • Hanukoglu I, Hanukoglu A (2016). "Epithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseases". Gene. 579 (2): 95–132. doi:10.1016/j.gene.2015.12.061. PMC 4756657. PMID 26772908.
  • Hanukoglu A, Vargas-Poussou R, Landau Z, Yosovich K, Hureaux M, Zennaro MC (2020). "Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 gene". J Steroid Biochem Mol Biol. 204: 105755. doi:10.1016/j.jsbmb.2020.105755. PMID 33017655.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)

ncbi.nlm.nih.gov