Muscle & Nerve

Cover image for Muscle & Nerve

Supplement: Muscle & Nerve

1995

Volume 18, Issue S14

Pages fmi–fmi, i–i, S1–S174

  1. Masthead

    1. Top of page
    2. Masthead
    3. Announcement from the Publisher
    4. Guest Editorials
    5. Articles
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181401

  2. Announcement from the Publisher

    1. Top of page
    2. Masthead
    3. Announcement from the Publisher
    4. Guest Editorials
    5. Articles
    1. Announcement from the publisher (page i)

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181402

  3. Guest Editorials

    1. Top of page
    2. Masthead
    3. Announcement from the Publisher
    4. Guest Editorials
    5. Articles
    1. Guest editorial (page S1)

      MD, PhD Seiichiro Tarui

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181403

  4. Articles

    1. Top of page
    2. Masthead
    3. Announcement from the Publisher
    4. Guest Editorials
    5. Articles
    1. Biochemistry and molecular genetics of human glycogenoses: An overview (pages S10–S17)

      Salvatore DiMauro, Seiichi Tsujino, Sara Shanske and Lewis P. Rowland

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181405

    2. McArdle's disease: Molecular genetics and metabolic consequences of the phenotype (pages S18–S22)

      Dr. Robert J. Beynon, Dr. Clare Bartram, Dr. Pam Hopkins, Dr. Veronica Toescu, Dr. Henry Gibson, Dr. Joanne Phoenix and Dr. Richard H. T. Edwards

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181406

    3. The molecular genetic basis of myophosphorylase deficiency (McArdle's disease) (pages S23–S27)

      Dr. Seiichi Tsujino, Dr. Sara Shanske, Dr. Ikuya Nonaka and Dr. Salvatore DiMauro

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181407

    4. Phosphofructokinase deficiency: Recent advances in molecular biology (pages S28–S34)

      Dr. Hiromu Nakajima, Dr. Tomoya Hamaguchi, Dr. Tomoyuki Yamasaki and Dr. Seiichiro Tarui

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181408

    5. Various classes of mutations in patients with phosphofructokinase deficiency (Tarui's disease) (pages S35–S38)

      Dr. Nina Raben, Dr. Jeffrey B. Sherman, Dr. Elizabeth Adams, Dr. Hiromu Nakajima, Dr. Zohar Argov and Dr. Paul Plotz

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181409

    6. A new variant case of muscle phosphofructokinase deficiency, coexisting with gastric ulcer, gouty arthritis, and increased hemolysis (pages S39–S44)

      Dr. Chisa Nakagawa, Dr. Ikuo Mineo, Dr. Misako Kaido, Dr. Harutoshi Fujimura, Dr. Takao Shimizu, Dr. Tomoya Hamaguchi, Dr. Hiromu Nakajima and Dr. Seiichiro Tarui

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181410

    7. Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency (pages S45–S49)

      Seiichi Tsujino, Sara Shanske and Salvatore DiMauro

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181411

    8. Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiency (pages S50–S53)

      Dr. Seiichi Tsujino, Dr. Sara Shanske, Dr. Saburo Sakoda, Dr. Antonio Toscano and Dr. Salvatore DiMauro

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181412

    9. Glycogenosis type II (acid maltase deficiency) (pages S61–S69)

      Dr. A. J. J. Reuser, Dr. M. A. Kroos, Dr. M. M. P. Hermans, Dr. A. G. A. Bijvoet, Dr. M. P. Verbeet, Dr. O. P. Van Diggelen, Dr. W. J. Kleijer and Dr. A. T. Van Der Ploeg

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181414

    10. Genetic defects in patients with glycogenosis type II (acid maltase deficiency) (pages S70–S74)

      Nina Raben, Ralph C. Nichols, Cornelius Boerkoel and Paul Plotz

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181415

    11. Leber's hereditary optic neuropathy among Japanese (pages S85–S89)

      Satoshi Ishikawa, Yoshiaki Ichibe, Junko Yokoe and Masato Wakakura

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181418

    12. Clinicopathological features of MERRF (pages S90–S94)

      Nobuyoshi Fukuhara

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181419

    13. Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas (pages S102–S106)

      Dr. Nils-Göran Larsson, Dr. Mar H. Tulinius, Dr. Elisabeth Holme and Dr. Anders Oldfors

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181421

    14. Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (pages S113–S118)

      Dr. Shuji Mita, Dr. Makoto Tokunaga, Dr. Toshihide Kumamoto, Dr. Makoto Uchino, Dr. Ikuya Nonaka and Dr. Masayuki Ando

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181423

    15. Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene (pages S119–S123)

      Dr. Yasutoshi Koga, Dr. Mercy Davidson, Dr. Eric A. Schon and Dr. Michael P. King

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181424

    16. Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation (pages S124–S130)

      Dr. J. M. W. van den Ouweland, Dr. H. H. P. J. Lemkes, Dr. K.-D. Gerbitz and Dr. J. A. Maassen

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181425

    17. Mitochondrial diabetes mellitus—glucose-induced signaling defects and β-cell loss (pages S131–S136)

      Dr. Yoshitomo Oka, Dr. Hideki Katagiri, Dr. Hisamitsu Ishihara, Dr. Tomoichiro Asano, Dr. Masatoshi Kikuchi and Dr. Tetsuro Kobayashi

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181426

    18. A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene (pages S137–S141)

      Dr. T. Kadowaki, Dr. H. Sakura, Dr. S. Otabe, Dr. K. Yasuda, Dr. H. Kadowaki, Dr. Y. Mori, Dr. R. Hagura, Dr. Y. Akanuma and Dr. Y. Yazaki

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181427

    19. A new mitochondrial DNA deletion associated with diabetic amyotrophy, diabetic myoatrophy and diabetic fatty liver (pages S142–S149)

      Dr. Yoshinori Hinokio, Dr. Susumu Suzuki, Dr. Koga Komatu, Dr. Masataka Ohtomo, Dr. Masatoshi Onoda, Dr. Masahiro Matsumoto, Dr. Satoshi Hirali, Dr. Yoshinori Sato, Dr. Hiroaki Akai, Dr. Koji Abe, Dr. Shigeaki Miyabayasi, Dr. Ryuzo Abe and Dr. Takayoshi Toyota

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181428

    20. Phenotype–genotype correlations in skeletal muscle of patients with mtDNA deletions (pages S150–S153)

      Dr. C. T. Moraes, Dr. M. Sciacco, Dr. E. Ricci, Dr. C. H. Tengan, Dr. H. Hao, Dr. E. Bonilla, Dr. E. A. Schon and Dr. S. DiMauro

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181429

    21. Duplications of mitochondrial DNA in Kearns–Sayre syndrome (pages S154–S158)

      Dr. Joanna Poulton, Dr. Karl J. Morten, Dr. David Marchington, Dr. Katharin Weber, Dr. Garry K. Brown, Dr. Agnès Rötig and Dr. Laurence Bindoff

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181430

    22. Mitochondrial DNA mutations in cardiomyopathy: Combination of replacements yielding cysteine residues and tRNA mutations (pages S165–S169)

      Masashi Tanaka, Toshihiro Obayashi, Makoto Yoneda, Sergey A. Kovalenko, Satoru Sugiyama and Takayuki Ozawa

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181432

    23. OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy (pages S170–S174)

      Dr. Massimo Zeviani, Dr. Caterina Mariotti, Dr. Carlo Antozzi, Dr. Giovanni Matteo Fratta, Dr. Pierre Rustin and Dr. Alessandro Prelle

      Version of Record online: 13 OCT 2004 | DOI: 10.1002/mus.880181433

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