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Journal Abstract Search

86 related items for PubMed ID: 3098698

  • 1. [Hereditary coproporphyria with grand mal epilepsy, glucose-6-phosphate dehydrogenase deficiency and phenobarbital tolerance].
    Grosser S, Klose G, Weisner B, Doss M.
    Internist (Berl); 1986 Oct; 27(10):672-6. PubMed ID: 3098698
    [No Abstract] [Full Text] [Related]

  • 2. Phenobarbital vs. phenytoin for grand mal epilepsy.
    Livingston S, Pauli LL, Pruce I, Kramer II.
    Am Fam Physician; 1980 Aug; 22(2):123-7. PubMed ID: 6773400
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  • 3. [Intravenous diazepam (Valium) in the treatment of mal epileptic states. A double blind study].
    Barbeau A.
    Int Z Klin Pharmakol Ther Toxikol; 1968 Aug; 1(6):550-7. PubMed ID: 4975961
    [No Abstract] [Full Text] [Related]

  • 4. [Autosomal dominant cerebral seizures in the 6th month of life with benign outcome].
    Kurlemann G, Vossschulte P, Weglage J, Palm DG.
    Klin Padiatr; 1995 Aug; 207(1):17-8. PubMed ID: 7885012
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  • 5. [Severe catatonia, schizophrenia and hereditary coproporphyria. A case report (author's transl)].
    Offenstadt G, Bienvenu MP, Héricord P, Tawill S, Amstutz P.
    Sem Hop; 1995 Aug; 56(41-42):1727-30. PubMed ID: 6255601
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  • 10. [Description of a case of a syndrome similar to Reye's syndrome in a male adult undergoing treatment with valproic acid and phenobarbital].
    Seghieri G, De Giorgio LA, Innocenti F, Pettiná G, Zolfanelli F, Apicella P.
    G Clin Med; 1982 Sep; 63(9):610-3. PubMed ID: 6819973
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  • 11. Effect of phenobarbital treatment on erythrocyte glucose-6-phosphate dehydrogenase in human newborns.
    Laconi E, Dessì S, Batetta B, Pani P, Pirisi L, Andria C, Macciotta A.
    Pediatr Pharmacol (New York); 1983 Sep; 3(2):59-62. PubMed ID: 6674910
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  • 13. [Grand mal status and grand mal series--causes, therapy and course].
    Fröscher W, Ansmann EB.
    Anasth Intensivther Notfallmed; 1985 Feb; 20(1):12-8. PubMed ID: 3922236
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  • 14. [Experience in the clinical use of K4-1152].
    Hayashi M, Shimazono Y.
    No To Shinkei; 1967 Mar; 19(3):251-6. PubMed ID: 4962894
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  • 16. [Clinical heterogeneity of hereditary coproporphyria: diagnostic usefulness of biochemical studies. Study of a familial case].
    Savi M, David S, Dall'Aglio P.
    Pathologica; 1983 Mar; 75 Suppl():134-7. PubMed ID: 6680417
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  • 17. [Changes in the excretory balance of urinary and fecal coproporphyrins in various cholestatic diseases].
    Arnalich Fernández F, Enríquez de Salamanca R, Catalán Beltrán T, Mas Andrés V, García Puig J.
    Rev Clin Esp; 1979 Oct 15; 155(1):13-7. PubMed ID: 538283
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  • 19. [Epilepsy with GTCs on awakening].
    Tanaka M, Inoue Y.
    Ryoikibetsu Shokogun Shirizu; 2002 Oct 15; (37 Pt 6):78-82. PubMed ID: 12483833
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