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The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention.

Ferreira CR, Regier DS, Yoon R, Pan KS, Johnston JM, Yang S, Spranger JW, Tifft CJ. Ferreira CR, et al. Among authors: spranger jw. Bone. 2020 Feb;131:115142. doi: 10.1016/j.bone.2019.115142. Epub 2019 Nov 6. Bone. 2020. PMID: 31704340 Free PMC article.

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Mixed-sclerosing-bone-dystrophy (osteopathia striata and osteopetrosis) and Cushing's syndrome.

Spranger J. Spranger J. Bone. 1991;12(2):133. doi: 10.1016/8756-3282(91)90012-8. Bone. 1991. PMID: 2064841 No abstract available.

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Ischiospinal dysostosis with rib gaps and nephroblastomatosis.

Spranger J, Self S, Clarkson KB, Pai GS. Spranger J, et al. Clin Dysmorphol. 2001 Jan;10(1):19-23. doi: 10.1097/00019605-200101000-00004. Clin Dysmorphol. 2001. PMID: 11152142 Review.

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PIGQ glycosylphosphatidylinositol-anchored protein deficiency: Characterizing the phenotype.

Starr LJ, Spranger JW, Rao VK, Lutz R, Yetman AT. Starr LJ, et al. Among authors: spranger jw. Am J Med Genet A. 2019 Jul;179(7):1270-1275. doi: 10.1002/ajmg.a.61185. Epub 2019 May 30. Am J Med Genet A. 2019. PMID: 31148362

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Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations.

Warren HE, Louie RJ, Friez MJ, Frías JL, Leroy JG, Spranger JW, Skinner SA, Champaigne NL. Warren HE, et al. Among authors: spranger jw. Clin Case Rep. 2018 Oct 15;6(11):2252-2255. doi: 10.1002/ccr3.1818. eCollection 2018 Nov. Clin Case Rep. 2018. PMID: 30455931 Free PMC article.

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Hyperostosis in siblings.

Spranger JW, Lausch E. Spranger JW, et al. S Afr Med J. 2016 May 25;106(6 Suppl 1):S98-9. doi: 10.7196/SAMJ.2016.v106i6.11007. S Afr Med J. 2016. PMID: 27245539

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Beyond osteogenesis imperfecta: Causes of fractures during infancy and childhood.

Bronicki LM, Stevenson RE, Spranger JW. Bronicki LM, et al. Among authors: spranger jw. Am J Med Genet C Semin Med Genet. 2015 Dec;169(4):314-27. doi: 10.1002/ajmg.c.31466. Epub 2015 Nov 4. Am J Med Genet C Semin Med Genet. 2015. PMID: 26531771 Review.

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A disorder resembling pseudoachondroplasia but without COMP mutation.

Spranger JW, Zabel B, Kennedy J, Jackson G, Briggs M. Spranger JW, et al. Am J Med Genet A. 2005 Jan 1;132A(1):20-4. doi: 10.1002/ajmg.a.30350. Am J Med Genet A. 2005. PMID: 15551305

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A new type of autosomal recessive spondyloepiphyseal dysplasia tarda.

Leroy JG, Leroy BP, Emmery LV, Messiaen L, Spranger JW. Leroy JG, et al. Among authors: spranger jw. Am J Med Genet A. 2004 Feb 15;125A(1):49-56. doi: 10.1002/ajmg.a.20419. Am J Med Genet A. 2004. PMID: 14755466

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Recessive omodysplasia: five new cases and review of the literature.

Elçioglu NH, Gustavson KH, Wilkie AO, Yüksel-Apak M, Spranger JW. Elçioglu NH, et al. Among authors: spranger jw. Pediatr Radiol. 2004 Jan;34(1):75-82. doi: 10.1007/s00247-003-1064-9. Epub 2003 Oct 18. Pediatr Radiol. 2004. PMID: 14566439 Review.

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