Literature DB >> 8970759

Growth hormone therapy in two patients with hereditary multiple exostosis.

C Galasso1, G Scirè, M L Sanna, S Carnazza, F Bonaiuto, B Boscherini.   

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Year:  1996        PMID： 8970759     DOI： 10.1177/000992289603501208

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN： 0009-9228            Impact factor:   1.168


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  3 in total

1.  Clinical and molecular studies of EXT1/EXT2 in Bulgaria.

Authors:  Malina Kirilova Stancheva-Ivanova; Wim Wuyts; Els van Hul; Briguita Ivanova Radeva; Radoslava Vasileva Vazharova; Todor Petrov Sokolov; Borislav Yordanov Vladimirov; Margarita Dimitrova Apostolova; Ivo Marinov Kremensky
Journal:  J Inherit Metab Dis       Date:  2011-04-16       Impact factor: 4.982

2.  Unusual location of osteochondroma in the temporal region in a patient with functional pituitary adenoma.

Authors:  Henry Olayere Obanife; Akaba Kingsley; John Ashindointiang; Joseph Asuquo; Olabisi Ogunleye; Iwasam E Joshua
Journal:  J Int Med Res       Date:  2021-12       Impact factor: 1.671

3.  Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

Authors:  Mauro Bozzola; Chiara Gertosio; Maria Gnoli; Federico Baronio; Elena Pedrini; Cristina Meazza; Luca Sangiorgi
Journal:  Ital J Pediatr       Date:  2015-08-04       Impact factor: 2.638
  3 in total

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