Literature DB >> 14197943

OSTEOGENESIS IMPERFECTA WITH ARTHROGRYPOSIS MULTIPLEX CONGENITA.

N L SHARMA, J S ANAND.   

Abstract

Keywords:  ABNORMALITIES; ARTHROGRYPOSIS; FETAL DISEASES; INFANT; INFANT, NEWBORN; LABOR PRESENTATION; OSTEOGENESIS IMPERFECTA; RADIOGRAPHY

Mesh：

Year:  1964        PMID： 14197943

Source DB:  PubMed          Journal:  J Indian Med Assoc        ISSN： 0019-5847


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  6 in total

1.  Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17.

Authors:  R A Bank; S P Robins; C Wijmenga; L J Breslau-Siderius; A F Bardoel; H A van der Sluijs; H E Pruijs; J M TeKoppele
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-02       Impact factor: 11.205

2.  Arthrogryposis multiplex congenita. Report of two cases.

Authors:  S Inamdar; B N Wala; R K Mansharamani; S Husain
Journal:  Indian J Pediatr       Date:  1967-12       Impact factor: 1.967

3.  Extraperitoneal laparoscopy-assisted percutaneous nephrolithotomy in a patient with osteogenesis imperfecta.

Authors:  Seref Basal; Yasar Ozgok; Lutfi Tahmaz; Abdulkadir Atim; Murat Zor; Serkan Bilgic; Okan Istanbulluoglu
Journal:  Urol Res       Date:  2010-03-14

4.  Bruck syndrome.

Authors:  Vikram Datta; Aditi Sinha; Arvind Saili; Sushma Nangia
Journal:  Indian J Pediatr       Date:  2005-05       Impact factor: 1.967

5.  Defective collagen fibril formation and mineralization in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome).

Authors:  R E Brenner; U Vetter; H Stöss; P K Müller; W M Teller
Journal:  Eur J Pediatr       Date:  1993-06       Impact factor: 3.183

6.  Osteogenesis imperfecta in childhood: cardiac and renal manifestations.

Authors:  U Vetter; B Maierhofer; M Müller; D Lang; W M Teller; R Brenner; D Frohneberg; O Wörsdörfer
Journal:  Eur J Pediatr       Date:  1989-12       Impact factor: 3.183
  6 in total

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