Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases

LETTER TO THE EDITOR

Satellite cell content in Huntington’s disease patients in response to endurance training

Sandro Manuel Mueller, Violeta Mihaylova, Sebastian Frese, Jens A. Petersen, Maria Ligon-Auer, David Aguayo, Martin Flück, Hans H. Jung and Marco Toigo

Orphanet Journal of Rare Diseases 2019, 14:135 | Published on: 11 June 2019

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LETTER TO THE EDITOR

Triglyceride deposit cardiomyovasculopathy: a rare cardiovascular disorder

Ming Li, Ken-ichi Hirano, Yoshihiko Ikeda, Masahiro Higashi, Chikako Hashimoto, Bo Zhang, Junji Kozawa, Koichiro Sugimura, Hideyuki Miyauchi, Akira Suzuki, Yasuhiro Hara, Atsuko Takagi, Yasuyuki Ikeda, Kazuhiro Kobayashi, Yoshiaki Futsukaichi, Nobuhiro Zaima…

Orphanet Journal of Rare Diseases 2019, 14:134 | Published on: 11 June 2019

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REVIEW

Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines

K. Martin, S. Geuens, J. K. Asche, R. Bodan, F. Browne, A. Downe, N. García García, G. Jaega, B. Kennedy, P. J. Mauritz, F. Pérez, K. Soon, V. Zmazek and K. M. Mayre-Chilton

Orphanet Journal of Rare Diseases 2019, 14:133 | Published on: 11 June 2019

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RESEARCH

Phenotypic variation between siblings with Metachromatic Leukodystrophy

Saskia Elgün, Jakob Waibel, Christiane Kehrer, Diane van Rappard, Judith Böhringer, Stefanie Beck-Wödl, Jennifer Just, Ludger Schöls, Nicole Wolf, Ingeborg Krägeloh-Mann and Samuel Groeschel

Orphanet Journal of Rare Diseases 2019, 14:136 | Published on: 11 June 2019

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