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Family Studies of Patients with Acute Intermittent Porphyria (AIP): Neurological, Biochemical, and Genetic Investigations

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Diagnosis and Therapy of Porphyrias and Lead Intoxication

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Abstract

Family studies beginning with four patients suffering from AIP were carried out, partly extending to the third generation. The results of the clinical, neurologic, biochemical, and genetic-enzymic investigations are reported and discussed here.

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References

  1. Doss, M., Meinhof, W.: Differenzierung hepatischer Porphyrien. Dtsch. Med. Wochenschr. 96, 1006–1013 (1971)

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Authors and Affiliations

  1. Department of Neurology, University Hospital Eppendorf, Hamburg, Germany

    K. F. Leonhardt

  2. Clinical Biochemistry of the University, Marburg a.L., Germany

    R. v. Tiepermann & M. Doss

Authors
  1. K. F. Leonhardt
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  2. R. v. Tiepermann
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  3. M. Doss
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Editor information

Editors and Affiliations

  1. Department of Clinical Biochemistry, Faculty of Medicine, Philipp University of Marburg, Pilgrimstein 2, D-3550, Marburg, Federal Republic of Germany

    Manfred Doss

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© 1978 Springer-Verlag Berlin Heidelberg

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Leonhardt, K.F., v. Tiepermann, R., Doss, M. (1978). Family Studies of Patients with Acute Intermittent Porphyria (AIP): Neurological, Biochemical, and Genetic Investigations. In: Doss, M. (eds) Diagnosis and Therapy of Porphyrias and Lead Intoxication. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67002-2_13

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  • DOI: https://doi.org/10.1007/978-3-642-67002-2_13

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-08863-9

  • Online ISBN: 978-3-642-67002-2

  • eBook Packages: Springer Book Archive

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