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LA COPROPORPHYRIE HEREDITAIRE. SEPT OBSERVATIONS.JAEGER A; TEMPE JD; GEISLER F et al.1975; NOUV. PRESSE MED.; FR.; DA. 1975; VOL. 4; NO 39; PP. 2783-2787; ABS. ANGL.; BIBL. 25 REF.Article

ROTOR'S SYNDROME. A DISTINCT INHERITABLE PATHOPHYSIOLOGIC ENTITYWOLKOFF AW; WOLPERT E; PASCASIO FN et al.1976; AMER. J. MED.; U.S.A.; DA. 1976; VOL. 60; NO 2; PP. 173-179; BIBL. 1 P.Article

URINARY EXCRETION OF 17-OXOSTEROIDS IN HEREDITARY COPROPORPHYRIAPAXTON JW; MOORE MR; BEATTIE AD et al.1975; CLIN. SCI. MOLEC. MED.; G.B.; DA. 1975; VOL. 49; NO 5; PP. 441-444; BIBL. 10 REF.Article

COPPER COPROPORPHYRIN EXCRETION IN FAMILIAL COPROPORPHYRIACARLSON RE; DOLPHIN D; BERNSTEIN M et al.1978; CLIN. CHEM.; USA; DA. 1978; VOL. 24; NO 11; PP. 2009-2012; BIBL. 9 REF.Article

HEREDITARY COPROPORPHYRIA. DEMONSTRATION OF THE ABNORMALITIES IN HAEM BIOSYNTHESIS IN PERIPHERAL BLOOD.BRODIE MJ; THOMPSON GG; MOORE MR et al.1977; QUART. J. MED.; G.B.; DA. 1977; VOL. 46; NO 182; PP. 229-241; BIBL. 35 REF.Article

LA COPROPORPHYRIE HEPATIQUE HEREDITAIRE: A PROPOS DE DEUX CAS FAMILIAUX.DE SOMER LEROY ROXANE.sd; FRA; DA. S.D.; 947; 92-XI P.; 30 CM; BIBL. 90 P.; TH.: MED./ROUEN/1978Thesis

THE PRIMARY ENZYME DEFECT IN HEREDITARY COPROPORPHYRIA.ELDER GH; EVANS JO; THOMAS N et al.1976; LANCET; G.B.; DA. 1976; NO 7997; PP. 1217-1219; BIBL. 27 REF.Article

Induction of anaesthesia with ketamine during an acute crisis of hereditary coproporphyriaCAPOUET, V; DERNOVOI, B; AZAGRA, J. S et al.Canadian journal of anaesthesia. 1987, Vol 34, Num 4, pp 388-390, issn 0832-610XArticle

PREGNANCY AND THE ACUTE PORPHYRIAS.BRODIE MJ; MOORE MR; THOMPSON GC et al.1977; BRIT. J. OBSTETR. GYNAECOL.; G.B.; DA. 1977; VOL. 84; NO 10; PP. 726-731; BIBL. 28 REF.Article

CATATONIE GRAVE, SCHIZOPHRENIE ET COPROPORPHYRIE HEREDITAIREOFFENSTADT G; BIENVENU MP; HERICORD P et al.1980; SEM. HOP.; ISSN 0037-1777; FRA; DA. 1980; VOL. 56; NO 41-42; PP. 1727-1730; ABS. ENG; BIBL. 25 REF.Article

DECREASED LYMPHOCYTE COPROPORPHYRINOGEN III OXIDASE ACTIVITY IN HEREDITARY COPROPORPHYRIA.GRANDCHAMP B; NORDMANN Y.1977; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1977; VOL. 74; NO 3; PP. 1089-1095; BIBL. 18 REF.Article

COEXISTENCE OF HEREDITARY COPROPORPHYRIA AND EPILEPSY: COPROPORPHYRINOGEN OXIDASE DEFICIENCY IN LIVER AND KIDNEYDOSS M; VON TIEPERMANN R; PFLUEGER KH et al.1981; J. NEUROL.; DEU; DA. 1981; VOL. 226; NO 1; PP. 25-33; BIBL. 31 REF.Article

PORPHYRIASBHUTANI LK; KUMAR AS.1981; INT. J. DERMATOL.; ISSN 0011-9059; USA; DA. 1981; VOL. 20; NO 5; PP. 380-384Article

HEREDITARY COPROPORPHYRIA AND EPILEPSY.HOUSTON AB; BRODIE MJ; MOORE MR et al.1977; ARCH. DIS. CHILDH.; G.B.; DA. 1977; VOL. 52; NO 8; PP. 646-650; BIBL. 28 REF.Article

LA COPROPORPHYRIE HEREDITAIRE. PRESENTATION D'UNE OBSERVATION. ETUDE GENETIQUE.TREDAN G.1976; ; S.L.; DA. 1976; PP. 1-145; BIBL. 15 P. 1/2; (THESE DOCT. MED.; RENNES)Thesis

LES PORPHYRIES CUTANEESHOMAREAU DIEULANGARD S; CIVATTE J.1978; REV. PRATICIEN; FRA; DA. 1978; VOL. 28; NO 47; PP. 3591-3607; (9 P.); ABS. ENG; BIBL. 10 REF.Article

Hereditary coproporphyria: unusual nervous system involvement in two casesCASALI, C; MONACO, M. L; D'ALESSANDRO, L et al.Journal of neurology. 1984, Vol 231, Num 2, pp 99-101, issn 0340-5354Article

Hereditary coproporphyria : a case reportSOMCHAI INSIRIPONG; PENPUN TULAYALAK; RATTAPORN UNGPAKORN et al.Chot Mai Het Thang Phaet. 1993, Vol 76, Num 1, pp 53-55, issn 0125-2208Article

Eruption à type d'Hydroa vacciniforme, révélatrice d'une coproporphyrie héréditaire = Hydroa vacciniform like eruption revealing hereditary coproporphyriaJEANMOUGIN, M; PEDREIRO, J; MANCIET, J.-R et al.Annales de dermatologie et de vénéréologie. 1988, Vol 115, Num 11, pp 1236-1238, issn 0151-9638Conference Paper

FAECAL PORPHYRIN EXCRETION IN VARIOUS TYPES OF PORPHYRIA: THIN LAYER CHROMATOGRAPHIC STUDYPERROT H; BOUCHERAT M; THIVOLET J et al.1978; ARCH. DERMATOL. RES.; DEU; DA. 1978; VOL. 263; NO 1; PP. 67-73; ABS. GER; BIBL. 23 REF.Article

Psychiatric manifestations of hereditary coproporphyria in a childMANDOKI, M. W; SUMNER, G. S.The Journal of nervous and mental disease. 1994, Vol 182, Num 2, pp 117-118, issn 0022-3018Article

Effects of erythromycin on gut transit in pseudo-obstruction due to hereditary coproporphyriaVASSALLO, M. J; CAMILLERI, M; SULLIVAN, S. N et al.Journal of clinical gastroenterology. 1992, Vol 14, Num 3, pp 255-259, issn 0192-0790Article

Haem arginate in acute hereditary coproporphyriaMANNING, D. J; GRAY, T. A.Archives of disease in childhood. 1991, Vol 66, Num 6, pp 730-731, issn 0003-9888Article

Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyriaSCHMITT, Caroline; GOUYA, Laurent; GRANDCHAMP, Bernard et al.Human molecular genetics (Print). 2005, Vol 14, Num 20, pp 3089-3098, issn 0964-6906, 10 p.Article

Family study of acute intermittent porphyria and hereditary coproporphyria in Niigata and Akita Prefectures, JapanSASAKI, H; KANEKO, K; TSUNEYAMA, H et al.Journal of clinical epidemiology. 1996, Vol 49, Num 10, pp 1117-1123, issn 0895-4356Article

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