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Journal of Internal Medicine

Cover image for Journal of Internal Medicine

January 2001

Volume 249, Issue 1

Pages 1–108

  1. Reviews

    1. Top of page
    2. Reviews
    3. Original Articles
    4. Case Reports
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      Substance P: a pioneer amongst neuropeptides (pages 27–40)

      T. Hökfelt, B. Pernow and J. Wahren

      Version of Record online: 20 DEC 2001 | DOI: 10.1046/j.0954-6820.2000.00773.x

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  2. Original Articles

    1. Top of page
    2. Reviews
    3. Original Articles
    4. Case Reports
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      Unintentional weight loss: diagnosis and prognosis. The first prospective follow-up study from a secondary referral centre (pages 41–46)

      P. G. Lankisch, 1 M. Gerzmann, 1 J.-F. Gerzmann and 1 D. Lehnick 1,2

      Version of Record online: 9 OCT 2008 | DOI: 10.1046/j.1365-2796.2001.00771.x

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      Quality of life of chronic stable angina patients 4 years after coronary angioplasty or coronary artery bypass surgery (pages 47–57)

      B. Brorsson, S. J. Bernstein, R. H. Brook and L. Werkö

      Version of Record online: 9 OCT 2008 | DOI: 10.1046/j.1365-2796.2001.00782.x

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      Angiotensin-converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis (pages 77–83)

      M. Schürmann, 1 P. Reichel, 1 B. Müller-Myhsok, 2 T. Dieringer, 3 K. Wurm, 3 M. Schlaak, 4 J. Müller-Quernheim and 4 E. Schwinger 1

      Version of Record online: 9 OCT 2008 | DOI: 10.1046/j.1365-2796.2001.00776.x

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      Familial phosphofructokinase deficiency is associated with a disturbed calcium homeostasis in erythrocytes (pages 85–95)

      G. Ronquist, O. Rudolphi, I. Engström and A. Waldenström

      Version of Record online: 9 OCT 2008 | DOI: 10.1046/j.1365-2796.2001.00780.x

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      Increased erythrocyte content of Ca2+ in patients with Tarui's disease (pages 97–102)

      A. Waldenström, I. Engström and G. Ronquist

      Version of Record online: 9 OCT 2008 | DOI: 10.1046/j.1365-2796.2001.00779.x

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  3. Case Reports

    1. Top of page
    2. Reviews
    3. Original Articles
    4. Case Reports
    1. You have free access to this content
      Ehlers–Danlos syndrome type IV with a unique point mutation in COL3A1 and familial phenotype of myocardial infarction without organic coronary stenosis (pages 103–108)

      Y. Nishiyama, J. Nejima, A. Watanabe, E. Kotani, N. Sakai, A. Hatamochi, H. Shinkai, K. Kiuchi, K. Tamura, T. Shimada, T. Takano and Y. Katayama

      Version of Record online: 9 OCT 2008 | DOI: 10.1046/j.1365-2796.2001.00761.x

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