𝔖 Bobbio Scriptorium
✦   LIBER   ✦

TYPE-II GM1 GANGLIOSIDOSIS ?

✍ Scribed by Kint, J.A.; Dacremont, G.; Vlietinck, R.


Book ID
121982976
Publisher
The Lancet
Year
1969
Tongue
English
Weight
297 KB
Volume
294
Category
Article
ISSN
0140-6736

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


GM1-gangliosidosis type I
✍ Jiri Pavlu; Marie Jackson; Nicki Panoskaltsis πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 169 KB
Mongolian spots and GM1 type 1 gangliosi
✍ Burton Esterly, Nancy; Weissbluth, Marc; Caro, William A. πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 English βš– 182 KB
Clinical features of GM1 gangliosidosis
✍ Mano, T.; Matsuda, S.; Taira, M.; Yamamoto, T.; Shimizu, J.; Iwata, A.; Tsuji, S πŸ“‚ Article πŸ“… 2013 πŸ› Elsevier Science 🌐 English βš– 59 KB
Ovine GM1 gangliosidosis
✍ R.D. Murnane; A.J. Ahern-Rindell; D.J. Prieur πŸ“‚ Article πŸ“… 1991 πŸ› Elsevier Science 🌐 English βš– 898 KB
Dystonia and parkinsonism in GM1 type 3
✍ Emmanuel Roze; Eduard Paschke; Nathalie Lopez; Thomas Eck; Kunihiro Yoshida; Ann πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 84 KB

## Abstract GM1 gangliosidosis is due to β‐galactosidase deficiency. Only patients with type 3 disease survive into adulthood and develop movement disorders. Clinical descriptions of this form are rare, particularly in non‐Japanese patients. We describe four new patients and systematically analyze