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Issue |
Title |
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Vol 2, No 3 (2015): Supplement 3 |
Proceedings From The 10Th International Conference On Rare Diseases And Orphan Drugs (Icord). October 15-16, 2015 |
Abstract
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RARE Journal Secretariat |
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Vol 3, No 3 (2016): Supplement 1 |
Proceedings From The 11th International Conference On Rare Diseases And Orphan Drugs (ICORD). Cape Town, South Africa, 20-22 October, 2016 |
Abstract
PDF
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RARE Journal Secretariat |
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Vol 1: July 2014, Supplement 3 |
Proceedings from the IX International Conference on Rare Diseases and Orphan Drugs (ICORD). Ede (The Netherlands), October 7-9, 2014 |
Abstract
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Emilio Roldán, Annika Larsson, Désirée Gavhed |
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Vol 1: February 2014, Supplement 1 |
Proceedings from the VIII International Conference on Rare Diseases and Orphan Drugs (ICORD). St. Petersburg (Russia), October 31-November 2, 2013 |
Abstract
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Emilio José Antonio Roldán |
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Vol 1, No 2 (2014) |
Rare metabolic diseases among the Irish travellers: results from the All Ireland Traveller Health Study census and birth cohort (2007-2011) |
Abstract
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Noor Aman Hamid, Cecily Kelleher, Catherine McGorrian, Leslie Daly, Patricia Fitzpatrick |
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Vol 1, No 1 (2014) |
RARE-Bestpractices: a platform for sharing best practices for the management of rare diseases |
Abstract
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Domenica Taruscio, Cristina Morciano, Paola Laricchiuta, Pierpaolo Mincarone, RARE-Bestpractices Consortium |
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Vol 2, No 1 (2015) |
Report of an international workshop to explore the utility of the AGREE II instrument for appraisal of rare disease guidelines |
Abstract
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Michele Hilton Boon, Jenny Harbour, Karen Ritchie, Lorna Thompson |
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Vol 2, No 2 (2015) |
Rett Syndrome and the Role of National Parent Associations within a European Context |
Abstract
PDF
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Gillian Townend, Eric Smeets, Dick van Waardenburg, Rob van der Stel, Mariёlle van den Berg, Henk van Kranen, Leopold Curfs |
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Vol 2, No 3 (2015) |
Shared decision making in rare diseases: an overview |
Abstract
PDF
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Jeanette Pérez-Ramos, Analía Abt-Sacks, Lilisbeth Perestelo-Pérez, Amado Rivero-Santana, Ana Toledo-Chávarri, Nerea González, Pedro Serrano-Aguilar |
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Vol 1, No 3 (2014) |
Social impact identified in and by the alpha-1 antitrypsin deficiency community |
Abstract
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Charlie Strange, Sara Wienke, Deirdre Walker, Marvin Sineath, James Quill, Barbara Warner, Lucinda Shore, Susan Flavin, Pamela Williams |
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Vol 1, No 4 (2014) |
The quest for diagnosis - a narrative analysis of patient journeys |
Abstract
PDF
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Edmund Jessop |
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Vol 2, No 1 (2015) |
The use of animal models in disease research |
Abstract
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Augusto Vitale, Flavia Chiarotti, Enrico Alleva |
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Vol 3, No 2 (2016) |
Use of the incomplete sentences and the ‘three wishes’ approach in the identification of the subjective perception and impact of cystic fibrosis. The first open methodological experience in Czech voluntary patients: a pilot study |
Abstract
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Jan Chrastina |
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Vol 2, No 2 (2015) |
Vol. 2, Number 2, 2015 |
Abstract
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RARE Journal |
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Vol 2, No 3 (2015) |
Vol. 2, Number 3 (2015) |
Details
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RARE Journal Secretariat |
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Vol 3, No 1 (2016) |
Vol. 3, No 1 (2016) |
Details
PDF
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RARE Journal Secretariat |
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Vol 3, No 3 (2016) |
Vol. 3, No 3 (2016) |
Details
PDF
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RARE Journal Secretariat |
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Vol 4, No 1 (2017): Vol 4, No 1 (2017) |
Vol. 4, No 1 (2017) |
Details
PDF
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RARE Journal Secretariat |
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Vol 3, No 2 (2016) |
Vol.3, No 2 (2016) |
Details
PDF
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RARE Journal Secretariat |
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Vol 2, No 3 (2015) |
Walking with McArdle disease: alienation and solidarity in a rare disease journey |
Abstract
PDF
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Edmund Jessop |
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Vol 1, No 3 (2014) |
Women’s knowledge and periconceptional use of folic acid: data from three birth centers in Italy. |
Abstract
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Laura Lauria, Giulia Adinolfi, Francesca Bartolomeo, Emanuela Petruccelli, Michele Grandolfo |
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