Literature DB >> 4926047

Chronic idiopathic hyperphosphatasia associated with pseudoxanthoma elasticum.

S M Mitsudo.   

Abstract

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Year:  1971        PMID： 4926047

Source DB:  PubMed          Journal:  J Bone Joint Surg Am        ISSN： 0021-9355            Impact factor:   5.284


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  9 in total

1.  Unique coexpression in osteoblasts of broadly expressed genes accounts for the spatial restriction of ECM mineralization to bone.

Authors:  Monzur Murshed; Dympna Harmey; José Luis Millán; Marc D McKee; Gerard Karsenty
Journal:  Genes Dev       Date:  2005-04-15       Impact factor: 11.361

2.  Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK.

Authors:  Michael P Whyte; Cristina Tau; William H McAlister; Xiafang Zhang; Deborah V Novack; Virginia Preliasco; Eduardo Santini-Araujo; Steven Mumm
Journal:  Bone       Date:  2014-07-23       Impact factor: 4.398

3.  [Osteitis deformans (Paget)--or a tarda-type of a hereditary hyperphosphatasia (author's transl)].

Authors:  A Enderle; S von Gumppenberg
Journal:  Arch Orthop Trauma Surg       Date:  1979-07-31

Review 4.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

Review 5.  Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene.

Authors:  Giacomina Brunetti; Flaviana Marzano; Silvia Colucci; Annamaria Ventura; Luciano Cavallo; Maria Grano; Maria Felicia Faienza
Journal:  Endocrine       Date:  2012-05-26       Impact factor: 3.633

6.  Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.

Authors:  Forough Saki; Zohreh Karamizadeh; Shiva Nasirabadi; Steven Mumm; William H McAlister; Michael P Whyte
Journal:  J Bone Miner Res       Date:  2013-06       Impact factor: 6.741

7.  An autopsy case of pseudoxanthoma elasticum: histochemical characteristics.

Authors:  Katsuaki Miki; Takashi Yuri; Nobuhiko Takeda; Kazuya Takehana; Toshiji Iwasaka; Airo Tsubura
Journal:  Med Mol Morphol       Date:  2007-09-18       Impact factor: 2.309

Review 8.  Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease.

Authors:  Gary S Gottesman; Katherine L Madson; William H McAlister; Angela Nenninger; Deborah Wenkert; Steven Mumm; Michael P Whyte
Journal:  Am J Med Genet A       Date:  2016-01-14       Impact factor: 2.802

9.  Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7).

Authors:  Michael P Whyte; Philippe M Campeau; William H McAlister; G David Roodman; Nori Kurihara; Angela Nenninger; Shenghui Duan; Gary S Gottesman; Vinieth N Bijanki; Homer Sedighi; Deborah J Veis; Steven Mumm
Journal:  Bone       Date:  2020-04-13       Impact factor: 4.398
  9 in total

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