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Part 16: LYSOSOMAL DISORDERS

134:

Sphingolipid Activator Proteins, Konrad Sandhoff / Thomas Kolter / Klaus Harzer / Ute Schepers / Natascha Remmel [Abstract] [Full Text]
135:

Glycogen Storage Disease Type II: Acid α-Glucosidase (Acid Maltase) Deficiency, Rochelle Hirschhorn / Arnold J.J. Reuser [Abstract] [Full Text]
136:

The Mucopolysaccharidoses, Elizabeth F. Neufeld / Joseph Muenzer [Abstract] [Full Text]
137:

Pycnodysostosis: Cathepsin K Deficiency, Bruce D. Gelb / Dieter Brömme / Robert J. Desnick [Abstract] [Full Text]
138:

I-Cell Disease and Pseudo-Hurler Polydystrophy: Disorders of Lysosomal Enzyme Phosphorylation and Localization, Stuart Kornfeld / William S. Sly [Abstract] [Full Text]
138.1:

Mucolipidosis Type IV, Ehud Goldin / Susan A. Slaugenhaupt / Janine A. Smith / Raphael Schiffmann [Abstract] [Full Text]
139:

α-N- Acetylgalactosaminidase Deficiency: Schindler Disease, Robert J. Desnick / Detlev Schindler [Abstract] [Full Text]
140:

Disorders of Glycoprotein Degradation: α-Mannosidosis, β-Mannosidosis, Fucosidosis, and Sialidosis, George H. Thomas [Abstract] [Full Text]
141:

Aspartylglucosaminuria, Pertti Aula / Anu Jalanko / Leena Peltonen [Abstract] [Full Text]
142:

Acid Lipase Deficiency: Wolman Disease and Cholesteryl Ester Storage Disease, Gerd Assmann / Udo Seedorf [Abstract] [Full Text]
143:

Acid Ceramidase Deficiency: Farber Lipogranulomatosis, Thierry Levade / Konrad Sandhoff / Heike Schulze / Jeffrey A. Medin [Abstract] [Full Text] Revised—June 2009
144:

Niemann-Pick Disease Types A and B: Acid Sphingomyelinase Deficiencies, Edward H. Schuchman / Robert J. Desnick [Abstract] [Full Text]
145:

Niemann-Pick Disease Type C: A Lipid Trafficking Disorder, Marc C. Patterson / Marie T. Vanier / Kinuko Suzuki / Jill A. Morris / Eugene Carstea / Edward B. Neufeld / Joan E. Blanchette-Mackie / Peter G. Pentchev [Abstract] [Full Text]
146:

Gaucher Disease, Gregory A. Grabowski / Gregory A. Petsko / Edwin H. Kolodny [Abstract] [Full Text] Revised—July 2010
146.1:

Gaucher Disease: Phenotypic and Genetic Variation, Gregory A. Grabowski / Edwin H. Kolodny / Neal J. Weinreb / Barry E. Rosenbloom / Ainu Prakash-Cheng / Paige Kaplan / Joel Charrow / Gregory M. Pastores / Pramod K. Mistry [Abstract] [Full Text]
147:

Galactosylceramide Lipidosis: Globoid Cell Leukodystrophy (Krabbe Disease), Kinuko Suzuki / Yoshiyuki Suzuki / Kunihiko Suzuki / David A. Wenger [Abstract] [Full Text]
148:

Metachromatic Leukodystrophy, Jaak Jaeken / Volkmar Gieselmann / Kurt von Figura [Abstract] [Full Text]
149:

Multiple Sulfatase Deficiency and the Nature of the Sulfatase Family, John J. Hopwood / Andrea Ballabio [Abstract] [Full Text]
150:

α-Galactosidase A Deficiency: Fabry Disease, Christine M. Eng / Yiannis A. Ioannou / Robert J. Desnick [Abstract] [Full Text]
151:

β-Galactosidase Deficiency (β-Galactosidosis): G_M1 Gangliosidosis and Morquio B Disease, Yoshiyuki Suzuki / Eiji Nanba / Junichiro Matsuda / Katsumi Higaki / Akihiro Oshima [Abstract] [Full Text] Revised—July 2008
152:

Galactosialidosis, Alessandra d'Azzo / Generoso Andria / Pietro Strisciuglio / Hans Galjaard [Abstract] [Full Text]
153:

The GM2, Roy A. Gravel / Michael M. Kaback / Richard L. Proia / Konrad Sandhoff / Kinuko Suzuki / Kunihiko Suzuki [Abstract] [Full Text]
154:

The Neuronal Ceroid Lipofuscinoses, Leena Peltonen / Sandra L. Hofmann [Abstract] [Full Text]
154.1:

Autophagy and Human Genetic Disease, Benjamin R Underwood / Dunecan C O Massey / David C Rubinsztein [Abstract] [Full Text] New—October 2010