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    1. Cochon, AC; de Viale, LCS; de Catabbi, SCB
      Phospholipid alterations elicited by hexachlorobenzene in rat brain are strain-dependent and porphyria-independent

      COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY
    2. Kere, J
      Human population genetics: Lessons from Finland

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    3. Richard, E; Mendez, M; Mazurier, F; Morel, C; Costet, P; Xia, P; Fontanellas, A; Geronimi, F; Cario-Andre, M; Taine, L; Ged, C; Malik, P; de Verneuil, H; Moreau-Gaudry, F
      Gene therapy of a mouse model of protoporphyria with a self-inactivating erythroid-specific lentiviral vector without preselection

      MOLECULAR THERAPY
    4. Mazurier, F; Geronimi, F; Lamrissi-Garcia, I; Morel, C; Richard, E; Ged, C; Fontanellas, A; Moreau-Gaudry, F; Morey, M; de Verneuil, H
      Correction of deficient CD34(+) cells from peripheral blood after mobilization in a patient with congenital erythropoietic porphyria

      MOLECULAR THERAPY
    5. Elder, GH; Hift, RJ
      Treatment of acute porphyria

      HOSPITAL MEDICINE
    6. Stewart, SF; Day, CP
      Liver disorder and the HFE locus

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    7. Teixeira, PC; Onuki, J; Medeiros, MHG; Dornemann, D; Di Mascio, P
      DNA damage by 3,6-dihydropyrazine-2,5-dipropanoic acid, the cyclic dimerization product of 5-aminolevulinic acid

      BIOLOGICAL CHEMISTRY
    8. Gutierrez, PP; Kunitz, O; Wolff, C; Frank, J
      Diagnosis and treatment of the acute porphyrias: An interdisciplinary challenge

      SKIN PHARMACOLOGY AND APPLIED SKIN PHYSIOLOGY
    9. Chaufan, G; de Molina, MDR; de Viale, LCS
      How does hexachlorobenzene treatment affect liver uroporphyrinogen decarboxylase?

      INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
    10. Brudieux, E; de Ledinghen, V; Moran, MJ; Fontanellas, A; Oui, B; Trimoulet, P; Belleannee, G; Piton, A; Raymond, JM; Doutre, MS; Amouretti, M; de Verneuil, H; Couzigou, P
      Hepatic porphyrin concentration and uroporphyrinogen decarboxylase activity in hepatitis C virus infection

      JOURNAL OF VIRAL HEPATITIS
    11. Spiewak, R
      Pesticides as a cause of occupational skin diseases in farmers

      ANNALS OF AGRICULTURAL AND ENVIRONMENTAL MEDICINE
    12. Corrigall, AV; Hift, RJ; Davids, LM; Hancock, V; Meissner, D; Kirsch, RE; Meissner, PN
      Identification of the first variegate porphyria mutation in an indigenous black South African and further evidence for heterogeneity in variegate porphyria

      MOLECULAR GENETICS AND METABOLISM
    13. Whysner, J; Wang, CX
      Hepatocellular iron accumulation and increased cell proliferation in polychlorinated biphenyl-exposed Sprague-Dawley rats and the development of hepatocarcinogenesis

      TOXICOLOGICAL SCIENCES
    14. Daikha-Dahmane, F; Dommergues, M; Narcy, F; Gubler, MC; Dumez, Y; Gauthier, E; Nordmann, Y; Nessmann, C; Terrasse, G; Muller, F
      Congenital erythropoietic porphyria: Prenatal diagnosis and autopsy findings in two sibling fetuses

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    15. Fargion, S; Stazi, MA; Fracanzani, AL; Mattioli, M; Sampietro, M; Tavazzi, D; Bertelli, C; Patriarca, V; Mariani, C; Fiorelli, G
      Mutations in the HFE gene and their interaction with exogenous risk factors in hepatocellular carcinoma

      BLOOD CELLS MOLECULES AND DISEASES
    16. Lucotte, G
      Frequency analysis and allele map in favor of the Celtic origin of the C282Y mutation of hemochromatosis

      BLOOD CELLS MOLECULES AND DISEASES
    17. Kotze, MJ; de Villiers, JNP; Rooney, RN; Grobbelaar, JJ; Mansvelt, EPG; Bouwens, CSH; Carr, J; Stander, I; du Plessis, L
      Analysis of the NRAMP1 gene implicated in iron transport: Association withmultiple sclerosis and age effects

      BLOOD CELLS MOLECULES AND DISEASES
    18. Gochee, PA; Powell, LW
      What's new in hemochromatosis

      CURRENT OPINION IN HEMATOLOGY
    19. Sykes, RM
      Acute intermittent porphyria, seizures, and antiepileptic drugs: a report on a 3-year-old Nigerian boy

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    20. Whitfield, JB
      Gamma glutamyl transferase

      CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES
    21. Barzilay, D; Orion, E; Brenner, S
      Porphyria cutanea tarda triggered by a combination of three predisposing factors

      DERMATOLOGY
    22. Granel, B; Serratrice, J; Bouabdallah, R; Pache, X; Weiller-Merli, C; Swiader, L; Aquaron, R; Disdier, P; Nordmann, Y; Weiller, PJ
      Atypical porphyria cutanea tarda in a patient with chronic myelogenous leukemia

      DERMATOLOGY
    23. Pozzato, G; Zorat, F; Nascimben, F; Gregorutti, M; Comar, C; Baracetti, S; Vatta, S; Bevilacqua, E; Belgrano, A; Crovella, S; Amoroso, A
      Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry

      EUROPEAN JOURNAL OF HUMAN GENETICS
    24. Fontanellas, A; Mendez, M; Mazurier, F; Cario-Andre, M; Navarro, S; Ged, C; Taine, L; Geronimi, F; Richard, E; Moreau-Gaudry, F; de Salamanca, RE; de Verneuil, H
      Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells

      GENE THERAPY
    25. Roy, CN; Andrews, NC
      Recent advances in disorders of iron metabolism: mutations, mechanisms andmodifiers

      HUMAN MOLECULAR GENETICS
    26. Grieco, A; Alfei, B; Di Rocco, P; Miele, L; Biolcati, G; Griso, D; Vecchio, FM; Bianco, A; Gasbarrini, G
      Non-alcoholic steatohepatitis induced by carbamazepine and variegate porphyria

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    27. Tannapfel, A; Stolzel, U; Kostler, E; Melz, S; Richter, M; Keim, V; Schuppan, D; Wittekind, C
      C282Y and H63D mutation of the hemochromatosis gene in German porphyria cutanea tarda patients

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    28. Forget, F; Awada, A; Klastersky, J
      Anticancer chemotherapy in a patient with prior history of acute intermittent porphyria - A case report and review of the literature

      SUPPORTIVE CARE IN CANCER
    29. McKane, W; Green, CA; Farrington, K
      Porphyria cutanea tarda precipitated by intravenous iron in a haemodialysis patient

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    30. Shiono, Y; Ikeda, R; Hayashi, H; Wakusawa, S; Sanae, F; Takikawa, T; Imaizumi, Y; Yano, M; Yoshioka, K; Kawanaka, M; Yamada, G
      C282Y and H63D mutations in the HFE gene have no effect on iron overload disorders in Japan

      INTERNAL MEDICINE
    31. Sata, M; Nagao, Y
      Hepatitis virus and extrahepatic manifestations - Skin, mucosa, muscle, and hematopoietic organs

      INTERNAL MEDICINE
    32. Krijt, J; Krijtova, H; Sanitrak, J
      Effect of tiagabine and topiramate on porphyrin metabolism in an in vivo model of porphyria

      PHARMACOLOGY & TOXICOLOGY
    33. Obermayer-Straub, P; Manns, MP
      Hepatitis C and D, retroviruses and autoimmune manifestations

      JOURNAL OF AUTOIMMUNITY
    34. Dutra, F; Knudsen, FS; Curi, D; Bechara, EJH
      Aerobic oxidation of aminoacetone, a threonine catabolite: Iron catalysis and coupled iron release from ferritin

      CHEMICAL RESEARCH IN TOXICOLOGY
    35. Coto-Montes, A; Boga, JA; Tomas-Zapico, C; Rodriguez-Colunga, MJ; Martinez-Fraga, J; Tolivia-Cadrecha, D; Menedez, G; Hardeland, R; Tolivia, D
      Physiological oxidative stress model: Syrian hamster Harderian gland - Sexdifferences in antioxidant enzymes

      FREE RADICAL BIOLOGY AND MEDICINE
    36. Warnich, L; Waso, HFJ; Groenewald, IM; Bester, AE; de Villiers, JNP; Kotze, MJ; Lynch, AG; Louw, JH
      Single nucleotide polymorphisms of the protoporphyrinogen oxidase gene: inter-population heterogeneity of allelic variation

      MOLECULAR AND CELLULAR PROBES
    37. Van Beek, MJ; Piette, WW
      Antimalarials

      DERMATOLOGIC CLINICS
    38. Rickes, S; Lochs, H; Wermke, W
      Suspected liver metastases in a man with porphyria cutanea tarda

      MEDIZINISCHE KLINIK
    39. Horvath, ME; Faux, SP; Smith, AG; Blazovics, A; van der Looij, M; Feher, J; Cheeseman, KH
      Vitamin E protects against iron-hexachlorobenzene induced porphyria and formation of 8-hydroxydeoxyguanosine in the liver of C57BL/10ScSn mice

      TOXICOLOGY LETTERS
    40. Chow, KM; Hui, CF; Lam, CW; Morgan, RR; Whatley, SD; Richard, K; Wong, KS
      Clinical and genetic features of variegate porphyria in a Chinese patient

      CHINESE MEDICAL JOURNAL
    41. Kaido, M; Fukada, K; Moriya, M; Abe, K; Sakoda, S; Kondo, M; Yanagihara, T
      Porphyria with double errors in the heme biosynthetic pathway

      JOURNAL OF NEUROLOGY
    42. Downey, D
      Porphyria: the road not traveled

      MEDICAL HYPOTHESES
    43. Onozato, ML; Tojo, A; Kamijo, A; Taniguchi, S; Kimura, K; Goto, A; Fujita, T
      Tubulointerstitial nephritis associated with acute intermittent porphyria

      CLINICAL NEPHROLOGY
    44. Qi, WB; Reiter, RJ; Tan, DX; Manchester, LC; Calvo, JR
      Melatonin prevents delta-aminolevulinic acid-induced oxidative DNA damage in the presence of Fe2+

      MOLECULAR AND CELLULAR BIOCHEMISTRY
    45. Oubina, JR; Quarleri, JF; Sawicki, MA; Mathet, VL; Ruiz, V; Schroder, T; Mendez, M; Parera, V; Muramatsu, H; Battle, A; Cappa, SMG; Fainboim, HA
      Hepatitis C virus and GBV-C/hepatitis G virus in argentine patients with porphyria cutanea tarda

      INTERVIROLOGY
    46. Oubre, D; Cruz, J; Keung, Y
      Porphyria cutanea tarda in a patient with post-transplant MDS

      BONE MARROW TRANSPLANTATION
    47. Shaw, PH; Mancini, AJ; McConnell, JP; Brown, D; Kletzel, M
      Treatment of congenital erythropoietic porphyria in children by allogeneicstem cell transplantation: a case report and review of the literature

      BONE MARROW TRANSPLANTATION
    48. Mathews, MAA; Schubert, HL; Whitby, FG; Alexander, KJ; Schadick, K; Bergonia, HA; Phillips, JD; Hill, CP
      Crystal structure of human uroporphyrinogen III synthase

      EMBO JOURNAL
    49. Green, JJ; Manders, SM
      Pseudoporphyria

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    50. Bosserhoff, AK; Hellerbrand, C; Buettner, R
      Clinical and genetic aspects of hereditary hemochromatosis

      PATHOLOGE
    51. Twaddle, S; Wassif, WS; Deacon, AC; Peters, TJ
      Celiac disease in patients with variegate porphyria

      DIGESTIVE DISEASES AND SCIENCES
    52. Whitfield, JB; Zhu, G; Heath, AC; Powell, LW; Martin, NG
      Effects of alcohol consumption on indices of iron stores and of iron stores on alcohol intake markers

      ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
    53. Millward, LM; Kelly, P; Deacon, A; Senior, V; Peters, TJ
      Self-rated psychosocial consequences and quality of life in the acute porphyrias

      JOURNAL OF INHERITED METABOLIC DISEASE
    54. Gross, U; Sassa, S; Arndt, T; Doss, MO
      Survival of two patients with severe delta-aminolaevulinic acid dehydratase deficiency porphyria

      JOURNAL OF INHERITED METABOLIC DISEASE
    55. Auchincloss, S; Pridmore, S
      Vomiting, burns, and irrational behaviour

      LANCET
    56. Nuttall, KL
      Abnormal chromatographic patterns of porphyrins in urine

      ANNALS OF CLINICAL AND LABORATORY SCIENCE
    57. Gross, P; Madias, NE; Teplan, V; Eckardt, KU; Henschkowski, J
      Treatment of severe hyponatremia

      KIDNEY INTERNATIONAL
    58. Horvath, ME; Faux, SP; Blazovics, A; Feher, J
      Lipid and DNA oxidative damage in experimentally induced hepatic porphyriain C57BL/10ScSn mice

      ZEITSCHRIFT FUR GASTROENTEROLOGIE
    59. Smith, AG; Clothier, B; Carthew, P; Childs, NL; Sinclair, PR; Nebert, DW; Dalton, TP
      Protection of the Cyp1a2(-/-) null mouse against uroporphyria and hepatic injury following exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin

      TOXICOLOGY AND APPLIED PHARMACOLOGY
    60. Krivosheev, AB; Krivosheev, BN; Kuimov, AD
      Late cutaneous porphyria and lupus erythematosis

      TERAPEVTICHESKII ARKHIV
    61. Albalate, M; Farinas, MC; Octavio, JG; Perez, JH; Goicoechea, M; Caramelo, C
      Development of porphyria cutanea tarda in a hemodialysis patient after reactivation of hepatitis C virus infection

      NEPHRON
    62. Phillips, JD; Jackson, LK; Bunting, M; Franklin, MR; Thomas, KR; Levy, JE; Andrews, NC; Kushner, JP
      A mouse model of familial porphyria cutanea tarda

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    63. Ramos-Casals, M; Font, J; Ingelmo, M
      Prevalence and clinical significance of hepatitis C virus infection in systemic autoimmune diseases

      MEDICINA CLINICA
    64. Rubens, O; Logina, I; Kravale, I; Eglite, M; Donaghy, M
      Peripheral neuropathy in chronic occupational inorganic lead exposure: a clinical and electrophysiological study

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    65. Kauppinen, R; Timonen, K; Fraunberg, MVZ; Laitinen, E; Ahola, H; Tenhunen, R; Taketani, S; Mustajoki, P
      Homozygous variegate porphyria: 20 y follow-up and characterization of molecular defect

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    66. Deacon, AC; Elder, GH
      Front line tests for the investigation of suspected porphyria

      JOURNAL OF CLINICAL PATHOLOGY
    67. Niu, TH; Seielstad, M; Zeng, X; Li, G; Apffel, A; Hahnenberger, K; Xu, XP
      Detection of novel ALAD gene polymorphisms using denaturing high-performance liquid chromatography

      HUMAN BIOLOGY
    68. Aguilar-Martinez, P; Bismuth, M; Picot, MC; Thelcide, C; Pageaux, GP; Blanc, F; Blanc, P; Schved, JF; Larrey, D
      Variable phenotypic presentation of iron overload in H63D homozygotes: aregenetic modifiers the cause?

      GUT
    69. Bacon, BR
      Hemochromatosis: Diagnosis and management

      GASTROENTEROLOGY
    70. Gaida-Hommernick, B; Rieck, K; Runge, U
      Oxcarbazepine in focal epilepsy and hepatic porphyria: A case report

      EPILEPSIA
    71. Le Gac, G; Mura, C; Ferec, C
      Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC

      CLINICAL CHEMISTRY
    72. Mamet, R; Sztern, M; Rachmel, A; Stahl, B; Flusser, D; Schoenfeld, N
      Lead poisoning: A new biochemical perspective on the differentiation between acquired and hereditary neuroporphyria

      CLINICAL CHEMISTRY
    73. Christiansen, L; Bygum, A; Kaehne, M; Jensen, A; Horder, M; Petersen, NE
      Mutation screening of the entire coding region of the protoporphyrinogen oxidase gene using denaturing gradient gel electrophoresis and denaturing HPLC

      CLINICAL CHEMISTRY
    74. Lam, CW; Poon, PMK; Tong, SF; Lo, AWI; Lai, CK; Choi, KL; Tiu, SC; Chan, YW; Shek, CC
      Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC

      CLINICAL CHEMISTRY
    75. Ma, Y; Fracanzani, AL; Sampietro, M; Mattioli, M; Cheeseman, P; Williams, R; Mieli-Vergani, G; Vergani, D; Fargion, S
      Autoantibodies to human cytosol: a marker of sporadic porphyria cutanea tarda

      CLINICAL AND EXPERIMENTAL IMMUNOLOGY
    76. Koike, R; Iizuka, T; Watanabe, T; Miyasaka, N
      The GOR gene product cannot cross-react with hepatitis C virus in humans

      CLINICAL AND EXPERIMENTAL IMMUNOLOGY
    77. Lam, CW; Hui, KN; Poon, PMK; Luk, NM; Yuen, YP; Tong, SF; Lai, CK; Chan, YW; Lo, KK
      Novel splicing mutation of the PPOX gene (IVS10+1G -> A) detected by denaturing high-performance liquid chromatography

      CLINICA CHIMICA ACTA
    78. Coto-Montes, A; Boga, JA; Tomas-Zapico, C; Rodriguez-Colunga, MJ; Martinez-Fraga, J; Tolivia-Cadrecha, D; Menendez, G; Hardeland, R; Tolivia, D
      Porphyric enzymes in hamster Harderian gland, a model of damage by porphyrins and their precursors. A chronobiological study on the role of sex differences

      CHEMICO-BIOLOGICAL INTERACTIONS
    79. Kobus, SM; Wong, SGW; Marks, GS
      Isolation of regioisomers of N-alkylprotoporphyrin IX from chick embryo liver after treatment with porphyrinogenic xenobiotics

      CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
    80. Porter, JB
      Practical management of iron overload

      BRITISH JOURNAL OF HAEMATOLOGY
    81. Palmer, RA; Elder, GH; Barrett, DF; Keohane, SG
      Homozygous variegate porphyria: a compound heterozygote with novel mutations in the protoporphyrinogen oxidase gene

      BRITISH JOURNAL OF DERMATOLOGY
    82. Dereure, O; Aguilar-Martinez, P; Bessis, D; Perney, P; Vallat, C; Guillot, B; Blanc, F; Guilhou, JJ
      HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France

      BRITISH JOURNAL OF DERMATOLOGY
    83. Lee, SC; Yun, SJ; Lee, JB; Lee, SS; Won, YH
      A case of porphyria cutanea tarda in association with idiopathic myelofibrosis and CREST syndrome

      BRITISH JOURNAL OF DERMATOLOGY
    84. Takeuchi, H; Kondo, M; Daimon, M; Susa, S; Ueoka, K; Uemura, O; Togari, H
      Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism

      BLOOD
    85. Phillips, JD; Parker, TL; Schubert, HL; Whitby, FG; Hill, CP; Kushner, JP
      Functional consequences of naturally occurring mutations in human uroporphyrinogen decarboxylase

      BLOOD
    86. Maruno, M; Furuyama, K; Akagi, R; Horie, Y; Meguro, K; Garbaczewski, L; Chiorazzi, N; Doss, MO; Hassoun, A; Mercelis, R; Verstraeten, L; Harper, P; Floderus, Y; Thunell, S; Sassa, S
      Highly heterogeneous nature of delta-aminolevulinate dehydratase (ALAD) deficiencies in ALAD porphyria

      BLOOD
    87. Gross, U; Schurek, JO; Doss, M; Doss, MO
      Haem arginate interferes with estimation of carcinoembryonic antigen

      ANNALS OF CLINICAL BIOCHEMISTRY
    88. Worwood, M
      What is the role of genetic testing in diagnosis of haemochromatosis?

      ANNALS OF CLINICAL BIOCHEMISTRY
    89. Lamoril, J; Puy, H; Whatley, SD; Martin, C; Woolf, JR; Da Silva, V; Deybach, JC; Elder, GH
      Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria

      AMERICAN JOURNAL OF HUMAN GENETICS
    90. Shiono, Y; Wakusawa, S; Hayashi, H; Takikawa, T; Yano, M; Okada, T; Mabuchi, H; Kono, S; Miyajima, H
      Iron accumulation in the liver of male patients with Wilson's disease

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    91. Frank, J; Aita, VM; Ahmad, W; Lam, HM; Wolff, C; Christiano, AM
      Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from Chile

      HUMAN HEREDITY
    92. Lovy, MR; Starkebaum, G
      Rheumatic disorders associated with hepatitis C

      BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
    93. Steward, CG
      Stem cell transplantation for non-malignant disorders

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    94. Poynard, T; Ratziu, V; Benhamou, Y; Opolon, P; Cacoub, P; Bedossa, P
      Natural history of HCV infection

      BEST PRACTICE & RESEARCH IN CLINICAL GASTROENTEROLOGY
    95. Venkatesh, P; Garg, SP; Kumaran, E; Tewari, HK
      Congenital porphyria with necrotizing scleritis in a 9-year-old child

      CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    96. Zuijderhoudt, FMJ; Koehorst, SGA; Kluitenberg, WE; Dorresteijn-de Bok, J
      On accuracy and precision of a HPLC method for measurement of urine porphyrin concentrations

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    97. Yu, S; Poulos, V; Stewart, P
      A novel mutation in a family with non-erythroid variant form of acute intermittent porphyria

      JOURNAL OF HUMAN GENETICS
    98. Maeda, N; Horie, Y; Adachi, K; Nanba, E; Kawasaki, H; Daimon, M; Kudo, Y; Kondo, M
      Two deletion mutations in the hydroxymethylbilane synthase gene in two unrelated Japanese patients with acute intermittent porphyria

      JOURNAL OF HUMAN GENETICS
    99. Dailey, HA; Dailey, TA; Wu, CK; Medlock, AE; Wang, KF; Rose, JP; Wang, BC
      Ferrochelatase at the millennium: structures, mechanisms and [2Fe-2S] clusters

      CELLULAR AND MOLECULAR LIFE SCIENCES
    100. Stewart, JM
      The cytoplasmic fatty-acid-binding proteins: thirty years and counting

      CELLULAR AND MOLECULAR LIFE SCIENCES


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Documento generato il 16/02/20 alle ore 23:26:12