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pro vyhledávání: '"Sana Eljamel"'
Autor:
Sana Eljamel, Wrik Ghosh, Sachin De Stone, Annabel Griffiths, Timothy Barrett, Richard Thompson
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-16 (2019)
Abstract Background Wolfram syndrome is a rare genetic, progressive, neurodegenerative disorder characterised by childhood-onset diabetes mellitus, diabetes insipidus, optic atrophy and deafness. To date, the economic burden of Wolfram syndrome has n
Externí odkaz:
https://doaj.org/article/2569b1a8e81f4dbe8ab1813dd58596bd
Autor:
Sana Eljamel, Annabel Griffiths, Jenni Evans, Indraneel Banerjee, Khalid Hussain, Richard Thompson
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-10 (2018)
Abstract Background Congenital hyperinsulinism (CHI) is a rare, genetic disease which causes persistent hypoglycaemia, typically in new-borns. Patients with the diffuse disease variant often require near-total surgical removal of the pancreas, causin
Externí odkaz:
https://doaj.org/article/da148f88ff984765ad6ab29b360cb001
Autor:
A Griffiths, Khalid Hussain, Indraneel Banerjee, Jenni Evans, Richard L. Thompson, Sana Eljamel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-10 (2018)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Congenital hyperinsulinism (CHI) is a rare, genetic disease which causes persistent hypoglycaemia, typically in new-borns. Patients with the diffuse disease variant often require near-total surgical removal of the pancreas, causing insulin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e16038571a154da25f1178c0d505d461
http://link.springer.com/article/10.1186/s13023-018-0867-6
http://link.springer.com/article/10.1186/s13023-018-0867-6