Sindrome di de Morsier (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrome di de Morsier" in Italian language version.

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12nih.gov

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Mutsuo Ishihara, Optic hypoplasia with pituitary dwarfism (Kaplan-Grumbach-Hoyt syndrome, or DeMorsier syndrome)., in Endocrinologia Japonica, vol. 30, n. 1, febbraio 1983, pp. 7–14, DOI:10.1507/endocrj1954.30.7, PMID 6884276. URL consultato l'11 ottobre 2012.
JB. Cruz, VS. Nunes; SA. Clara; D. Perone; P. Kopp; CR. Nogueira, Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency. (PDF), in Arq Bras Endocrinol Metabol, vol. 54, n. 5, 2010, pp. 482-7, DOI:10.1590/S0004-27302010000500009, PMID 20694410.
C. Mellado, A. Poduri; D. Gleason; PC. Elhosary; BJ. Barry; JN. Partlow; BS. Chang; GM. Shaw; AJ. Barkovich; CA. Walsh, Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort. (PDF), in Am J Med Genet A, 152A, n. 11, novembre 2010, pp. 2736-42, DOI:10.1002/ajmg.a.33684, PMID 20949537.
L. Zhao, SE. Zevallos; K. Rizzoti; Y. Jeong; et al., Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia., in Dev Cell, vol. 22, n. 3, marzo 2012, pp. 585-96, DOI:10.1016/j.devcel.2011.12.023, PMID 22421044.
CL. McMahon, SR. Braddock, Septo-optic dysplasia as a manifestation of valproic acid embryopathy., in Teratology, vol. 64, n. 2, agosto 2001, pp. 83-6, DOI:10.1002/tera.1049, PMID 11460259.
DE. McNay, JP. Turton; D. Kelberman; KS. Woods; et al., HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism. (PDF) ^{[collegamento interrotto]}, in J Clin Endocrinol Metab, vol. 92, n. 2, febbraio 2007, pp. 691-7, DOI:10.1210/jc.2006-1609, PMID 17148560.
Volpe JJ, Effect of cocaine use on the fetus, in N. Engl. J. Med., vol. 327, n. 6, agosto 1992, pp. 399–407, DOI:10.1056/NEJM199208063270607, PMID 1625714.

endojournals.org

jcem.endojournals.org

DE. McNay, JP. Turton; D. Kelberman; KS. Woods; et al., HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism. (PDF) ^{[collegamento interrotto]}, in J Clin Endocrinol Metab, vol. 92, n. 2, febbraio 2007, pp. 691-7, DOI:10.1210/jc.2006-1609, PMID 17148560.

jst.go.jp

jstage.jst.go.jp

Mutsuo Ishihara, Optic hypoplasia with pituitary dwarfism (Kaplan-Grumbach-Hoyt syndrome, or DeMorsier syndrome)., in Endocrinologia Japonica, vol. 30, n. 1, febbraio 1983, pp. 7–14, DOI:10.1507/endocrj1954.30.7, PMID 6884276. URL consultato l'11 ottobre 2012.

nih.gov

ncbi.nlm.nih.gov

Mutsuo Ishihara, Optic hypoplasia with pituitary dwarfism (Kaplan-Grumbach-Hoyt syndrome, or DeMorsier syndrome)., in Endocrinologia Japonica, vol. 30, n. 1, febbraio 1983, pp. 7–14, DOI:10.1507/endocrj1954.30.7, PMID 6884276. URL consultato l'11 ottobre 2012.
JB. Cruz, VS. Nunes; SA. Clara; D. Perone; P. Kopp; CR. Nogueira, Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency. (PDF), in Arq Bras Endocrinol Metabol, vol. 54, n. 5, 2010, pp. 482-7, DOI:10.1590/S0004-27302010000500009, PMID 20694410.
C. Mellado, A. Poduri; D. Gleason; PC. Elhosary; BJ. Barry; JN. Partlow; BS. Chang; GM. Shaw; AJ. Barkovich; CA. Walsh, Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort. (PDF), in Am J Med Genet A, 152A, n. 11, novembre 2010, pp. 2736-42, DOI:10.1002/ajmg.a.33684, PMID 20949537.
L. Zhao, SE. Zevallos; K. Rizzoti; Y. Jeong; et al., Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia., in Dev Cell, vol. 22, n. 3, marzo 2012, pp. 585-96, DOI:10.1016/j.devcel.2011.12.023, PMID 22421044.
CL. McMahon, SR. Braddock, Septo-optic dysplasia as a manifestation of valproic acid embryopathy., in Teratology, vol. 64, n. 2, agosto 2001, pp. 83-6, DOI:10.1002/tera.1049, PMID 11460259.
MS. Lubinsky, Hypothesis: septo-optic dysplasia is a vascular disruption sequence., in Am J Med Genet, vol. 69, n. 3, marzo 1997, pp. 235-6, PMID 9096749.
DE. McNay, JP. Turton; D. Kelberman; KS. Woods; et al., HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism. (PDF) ^{[collegamento interrotto]}, in J Clin Endocrinol Metab, vol. 92, n. 2, febbraio 2007, pp. 691-7, DOI:10.1210/jc.2006-1609, PMID 17148560.
Volpe JJ, Effect of cocaine use on the fetus, in N. Engl. J. Med., vol. 327, n. 6, agosto 1992, pp. 399–407, DOI:10.1056/NEJM199208063270607, PMID 1625714.
Dominguez R, Aguirre Vila-Coro A, Slopis JM, Bohan TP, Brain and ocular abnormalities in infants with in utero exposure to cocaine and other street drugs, in Am. J. Dis. Child., vol. 145, n. 6, giugno 1991, pp. 688–95, PMID 1709777.
Orrico A, Galli L, Zappella M, et al., Septo-optic dysplasia with digital anomalies associated with maternal multidrug abuse during pregnancy, in Eur. J. Neurol., vol. 9, n. 6, novembre 2002, pp. 679–82, PMID 12453085.
Barkovich AJ, Fram EK, Norman D, Septo-optic dysplasia: MR imaging, in Radiology, vol. 171, n. 1, aprile 1989, pp. 189–92, PMID 2928524.
Miller SP, Shevell MI, Patenaude Y, Poulin C, O'Gorman AM, Septo-optic dysplasia plus: a spectrum of malformations of cortical development, in Neurology, vol. 54, n. 8, aprile 2000, pp. 1701–3, PMID 10762523.

oadoi.org

L. Zhao, SE. Zevallos; K. Rizzoti; Y. Jeong; et al., Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia., in Dev Cell, vol. 22, n. 3, marzo 2012, pp. 585-96, DOI:10.1016/j.devcel.2011.12.023, PMID 22421044.
CL. McMahon, SR. Braddock, Septo-optic dysplasia as a manifestation of valproic acid embryopathy., in Teratology, vol. 64, n. 2, agosto 2001, pp. 83-6, DOI:10.1002/tera.1049, PMID 11460259.
Volpe JJ, Effect of cocaine use on the fetus, in N. Engl. J. Med., vol. 327, n. 6, agosto 1992, pp. 399–407, DOI:10.1056/NEJM199208063270607, PMID 1625714.

orpha.net

Displasia setto-ottica su orpha.net

scielo.br

JB. Cruz, VS. Nunes; SA. Clara; D. Perone; P. Kopp; CR. Nogueira, Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency. (PDF), in Arq Bras Endocrinol Metabol, vol. 54, n. 5, 2010, pp. 482-7, DOI:10.1590/S0004-27302010000500009, PMID 20694410.

whonamedit.com

(EN) Ole Daniel Enersen, Sindrome di de Morsier, in Who Named It?.