Lysosomal Websites
Verein Mukopolysaccharidosen Schweiz - Start
Die schweizerische Gesellschaft für Mukopolysaccharidosen ist eine Selbsthilfeorganisation, die von Eltern betroffener MPS-Patienten gegründet wurde. Seitdem ist der Verein gewachsen und inzwischen sind auch einige MPS Patienten selber im Verein aktiv. Neben MPS werden auch die Interessen von Patienten mit verwandten K
Not Applicable
$
8.94
laldaware
LAL Solace is an online support group to help patients with LAL Deficiency (Lysosomal Acid Lipase Disease) and Wolman Disease.
Not Applicable
$
8.95
MLD Foundation - The Premiere Family Resource for Metachromatic Leukod
Not Applicable
$
8.95
MLD Foundation - The Premiere Family Resource for Metachromatic Leukod
Not Applicable
$
8.95
MLD Foundation - The Premiere Family Resource for Metachromatic Leukod
Not Applicable
$
8.95
MLD Foundation - The Premiere Family Resource for Metachromatic Leukod
Not Applicable
$
8.95
MLD Foundation - The Premiere Family Resource for Metachromatic Leukod
Not Applicable
$
8.95
LAL Solace Patient Community - LAL Deficiency (Lysosomal Acid Lipase D
LAL Solace is an online support group to help patients with LAL Deficiency (Lysosomal Acid Lipase Disease) and Wolman Disease.
Not Applicable
$
8.95
MLD Foundation - The Premiere Family Resource for Metachromatic Leukod
9,408,246
$
240.00
laldaware
LAL Solace is an online support group to help patients with LAL Deficiency (Lysosomal Acid Lipase Disease) and Wolman Disease.
Not Applicable
$
8.95
LAL Solace Patient Community - LAL Deficiency (Lysosomal Acid Lipase D
LAL Solace is an online support group to help patients with LAL Deficiency (Lysosomal Acid Lipase Disease) and Wolman Disease.
Not Applicable
$
8.95
