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La ricerca find articoli where soggetti phrase all words 'X-LINKED ADRENOLEUKODYSTROPHY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 208 riferimenti
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    1. Luda, E; Barisone, MG
      Adult-onset adrenoleukodystrophy: a clinical and neuropsychological study

      NEUROLOGICAL SCIENCES
    2. Min, KT
      Drosophila as a model to study human brain degenerative diseases

      PARKINSONISM & RELATED DISORDERS
    3. Berger, J; Moser, HW; Forss-Petter, S
      Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment

      CURRENT OPINION IN NEUROLOGY
    4. McGuinness, MC; Zhang, HP; Smith, KD
      Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy

      MOLECULAR GENETICS AND METABOLISM
    5. Percy, AK; Rutledge, SL
      Adrenoleukodystrophy and related disorders

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    6. Kemp, S; Pujol, A; Waterham, HR; van Geel, BM; Boehm, CD; Raymond, GV; Cutting, GR; Wanders, RJA; Hugo, HW
      ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations

      HUMAN MUTATION
    7. Seedorf, U; Assmann, G
      The role of PPAR alpha in obesity

      NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
    8. Kaye, EM
      Update on genetic disorders affecting white matter

      PEDIATRIC NEUROLOGY
    9. Suzuki, Y; Imamura, A; Shimozawa, N; Kondo, N
      The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil

      BRAIN & DEVELOPMENT
    10. Bezman, L; Moser, AB; Raymond, GV; Rinaldo, P; Watkins, PA; Smith, KD; Kass, NE; Moser, HW
      Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

      ANNALS OF NEUROLOGY
    11. Carver, JD; Benford, VJ; Han, B; Cantor, AB
      The relationship between age and the fatty acid composition of cerebral cortex and erythrocytes in human subjects

      BRAIN RESEARCH BULLETIN
    12. Zhou, CJ; Zhao, LX; Inagaki, N; Guan, JL; Nakajo, S; Hirabayashi, T; Kikuyama, S; Shioda, S
      ATP-binding cassette transporter ABC2/ABCA2 in the rat brain: A novel mammalian lysosome-associated membrane protein and a specific marker for oligodendrocytes but not for myelin sheaths

      JOURNAL OF NEUROSCIENCE
    13. Reddy, JK; Hashimoto, T
      Peroxisomal beta-oxidation and peroxisome proliferator-activated receptor alpha: An adaptive metabolic system

      ANNUAL REVIEW OF NUTRITION
    14. Albet, S; Bentejac, M; Savary, S; Gondcaille, C; Netik, A; Berger, J; Szpirer, C; Troffer-Charlier, N; Bugaut, M
      Rat adrenoleukodystrophy-related (ALDR) gene: full-length cDNA sequence and new insight in expression

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    15. Schmidt, S; Haase, CG; Bezman, L; Moser, H; Schmidt, M; Kohler, W; Linington, C; Klockgether, T
      Serum autoantibody responses to myelin oligodendrocyte glycoprotein and myelin basic protein in X-linked adrenoleukodystrophy and multiple sclerosis

      JOURNAL OF NEUROIMMUNOLOGY
    16. Wilcken, B
      Rare diseases and the assessment of intervention: What sorts of clinical trials can we use?

      JOURNAL OF INHERITED METABOLIC DISEASE
    17. Zolman, BK; Silva, ID; Bartel, B
      The Arabidopsis pxa1 mutant is defective in an ATP-binding cassette transporter-like protein required for peroxisomal fatty acid beta-oxidation

      PLANT PHYSIOLOGY
    18. Baumann, N; Pham-Dinh, D
      Biology of oligodendrocyte and myelin in the mammalian central nervous system

      PHYSIOLOGICAL REVIEWS
    19. Bekiesinska-Figatowska, M; Tylki-Szymanska, A; Walecki, J; Stradomska, TJ
      MRI findings in an asymptomatic boy with X-linked adrenoleukodystrophy andhis symptomatic mother

      NEURORADIOLOGY
    20. O'Neill, GN; Aoki, M; Brown, RH
      ABCD1 translation-initiator mutation demonstrates genotype-phenotype correlation for AMN

      NEUROLOGY
    21. Krenn, M; Bonelli, RM; Niederwieser, G; Reisecker, F; Koltringer, P
      Adrenoleucodystrophy mimicking multiple sclerosis

      NERVENARZT
    22. Ito, M; Blumberg, BM; Mock, DJ; Goodman, AD; Moser, AB; Moser, HW; Smith, KD; Powers, JM
      Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: Morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    23. Ten, S; New, M; Maclaren, N
      Addison's disease 2001

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    24. Roerig, P; Mayerhofer, P; Holzinger, A; Gartner, J
      Characterization and functional analysis of the nucleotide binding fold inhuman peroxisomal ATP binding cassette transporters

      FEBS LETTERS
    25. Di Renzo, M; Laghi-Pasini, F; Dotti, MG; Formichi, P; Annunziata, A; Pasqui, AL; Pompella, G; Auteri, A; Federico, A
      Cytokine production from peripheral mononuclear cells in 2 patients affected by adrenomyeloneuropathy

      EUROPEAN NEUROLOGY
    26. Fourcade, S; Savary, S; Albet, S; Gauthe, D; Gondcaille, C; Pineau, T; Bellenger, J; Bentejac, M; Holzinger, A; Berger, J; Bugaut, M
      Fibrate induction of the adrenoleukodystrophy-related gene (ABCD2) - Promoter analysis and role of the peroxisome proliferator-activated receptor PPAR alpha

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    27. Girard, S; Bruckert, E; Turpin, G
      Endocrine disease in adrenoleukodystrophy

      ANNALES DE MEDECINE INTERNE
    28. Raggers, RJ; Pomorski, T; Holthuis, JCM; Kalin, N; van Meer, G
      Lipid traffic: The ABC of transbilayer movement

      TRAFFIC
    29. Seedorf, U; Ellinghaus, P; Nofer, JR
      Sterol carrier protein-2

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    30. Moser, HW
      Molecular genetics of peroxisomal disorders

      FRONTIERS IN BIOSCIENCE
    31. Porter, BE; Tennekoon, G
      Myelin and disorders that affect the formation and maintenance of this sheath

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    32. Lachtermacher, MBR; Seuanez, HN; Moser, AB; Moser, HW; Smith, KD
      Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described

      HUMAN MUTATION
    33. Hughes, JM; Whelan, MA; Deringer, PM
      Adrenoleukodystrophy: An important cause of adrenal insufficiency

      ENDOCRINOLOGIST
    34. Falorni, A; Laureti, S
      Adrenal autoimmunity and correlation with adrenal dysfunction

      ENDOCRINOLOGIST
    35. Feigenbaum, V; Gelot, A; Casanova, P; Daumas-Duport, C; Aubourg, P; Dubois-Dalcq, M
      Apoptosis in the central nervous system of cerebral adrenoleukodystrophy patients

      NEUROBIOLOGY OF DISEASE
    36. Pujol, A; Troffer-Charlier, N; Metzger, E; Chimini, G; Mandel, JL
      Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: Inductibility by retinoic acid and forskolin

      GENOMICS
    37. Aubourg, P
      Bone marrow transplantation in adrenoleucocystrophia

      M S-MEDECINE SCIENCES
    38. Luton, JP; Bertherat, J; Bertagna, X
      Familial diseases of the adrenal gland: progress in molecular medicine andrisks of genetic screening

      PRESSE MEDICALE
    39. Al-Essa, MA; Sakati, NA; Bakheet, SM; Patay, ZJ; Dabbagh, O; Chaves-Carballo, E; Ozand, PT
      X-linked adrenoleukodystrophy - The Saudi experience

      SAUDI MEDICAL JOURNAL
    40. Rizzo, WB
      Peroxisome 1, 2, 3 ...

      ANNALS OF NEUROLOGY
    41. Gartner, J
      Organelle disease: peroxisomal disorders

      EUROPEAN JOURNAL OF PEDIATRICS
    42. Izquierdo, M; Adamsbaum, C; Benosman, A; Aubourg, P; Bittoun, J
      MR spectroscopic imaging of normal-appearing white matter in adrenoleukodystrophy

      PEDIATRIC RADIOLOGY
    43. Vaidya, B; Pearce, S; Kendall-Taylor, P
      Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure

      CLINICAL ENDOCRINOLOGY
    44. Modebe, O
      Achalasia-Alacrima-ACTH insensitivity syndrome (triple A syndrome) in a Saudi family

      ANNALS OF SAUDI MEDICINE
    45. Stephenson, DJ; Bezman, L; Raymond, GV
      Acute presentation of childhood adrenoleukodystrophy

      NEUROPEDIATRICS
    46. Depreter, M; Tytgat, T; Beken, S; Espeel, M; De Smet, K; Rogiers, V; Roels, F
      Effects of extracellular matrix on the expression of peroxisomes in primary rat hepatocyte cultures

      JOURNAL OF HEPATOLOGY
    47. Yamada, T; Shinnoh, N; Taniwaki, T; Ohyagi, Y; Asahara, H; Horiuchi, I; Kira, J
      Lovastatin does not correct the accumulation of very long-chain fatty acids in tissues of adrenoleukodystrophy protein-deficient mice

      JOURNAL OF INHERITED METABOLIC DISEASE
    48. Netik, A; Hobel, A; Rauschka, H; Molzer, B; Forss-Petter, S; Berger, J
      Rolipram does not normalize very long-chain fatty acid levels in adrenoleukodystrophy protein-deficient fibroblasts and mice

      JOURNAL OF INHERITED METABOLIC DISEASE
    49. Gartner, J
      Disorders related to peroxisomal membranes

      JOURNAL OF INHERITED METABOLIC DISEASE
    50. Barmaki Pour, R; Stockler-Ipsiroglu, S; Hunneman, DH; Gahr, M; Korenke, GC; Pabst, W; Hanefeld, F; Peters, A
      Enhanced lymphocyte proliferation in patients with adrenoleukodystrophy treated with erucic acid (22 : 1)-rich triglycerides

      JOURNAL OF INHERITED METABOLIC DISEASE
    51. Riva, D; Bova, SM; Bruzzone, MG
      Neuropsychological testing may predict early progression of asymptomatic adrenoleukodystrophy

      NEUROLOGY
    52. Ohi, T; Takechi, S; Itokazu, N; Shiomi, K; Sugimoto, S; Antoku, Y; Kato, K; Sugimoto, T; Nakayama, T; Matsukura, S
      Two novel mutations in the adrenoleukodystrophy gene in two unrelated Japanese families and the long-term effect of bone marrow transplantation

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    53. Powers, JM; DeCiero, DP; Ito, M; Moser, AB; Moser, HW
      Adrenomyeloneuropathy: A neuropathologic review featuring its noninflammatory myelopathy

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    54. Steinberg, SJ; Morgenthaler, J; Heinzer, AK; Smith, KD; Watkins, PA
      Very long-chain acyl-CoA synthetases - Human "bubblegum" represents a new family of proteins capable of activating very long-chain fatty acids

      JOURNAL OF BIOLOGICAL CHEMISTRY
    55. Cartier, N; Guidoux, S; Rocchiccioli, F; Aubourg, P
      Simvastatin does not normalize very long chain fatty acids in adrenoleukodystrophy mice

      FEBS LETTERS
    56. Gloeckner, CJ; Mayerhofer, PU; Landgraf, P; Muntau, AC; Holzinger, A; Gerber, JK; Kammerer, S; Adamski, J; Roscher, AA
      Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    57. Jones, AH
      Medicine and the movies: Lorenzo's Oil at century's end

      ANNALS OF INTERNAL MEDICINE
    58. Moser, HW
      Molecular genetics of peroxisomal disorders

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    59. Paik, MJ; Lee, KO; Shin, HS
      Determination of very-long-chain fatty acids in serum by gas chromatography-nitrogen-phosphorus detection following cyanomethylation

      JOURNAL OF CHROMATOGRAPHY B
    60. Scriver, CR; Treacy, EP
      Is there treatment for "genetic" disease?

      MOLECULAR GENETICS AND METABOLISM
    61. Steinberg, SJ; Wang, SJ; McGuinness, MC; Watkins, PA
      Human liver-specific very-long-chain acyl-coenzyme A synthetase: cDNA cloning and characterization of a second enzymatically active protein

      MOLECULAR GENETICS AND METABOLISM
    62. Braiterman, LT; Watkins, PA; Moser, AB; Smith, KD
      Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expression

      MOLECULAR GENETICS AND METABOLISM
    63. Rosebush, PI; Garside, S; Levinson, AJ; Mazurek, MF
      The neuropsychiatry of adult-onset adrenoleukodystrophy

      JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES
    64. Perusi, C; Gomez-Lira, M; Mottes, M; Pignatti, PF; Bertini, E; Cappa, M; Vigliani, MC; Schiffer, D; Rizzuto, N; Salviati, A
      Two novel missense mutations causing adrenoleukodystrophy in Italian patients

      MOLECULAR AND CELLULAR PROBES
    65. Moser, AB; Kreiter, N; Bezman, L; Lu, SE; Raymond, GV; Naidu, S; Moser, HW
      Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls

      ANNALS OF NEUROLOGY
    66. Moser, AB; Jones, DS; Raymond, GV; Moser, HW
      Plasma and red blood cell fatty acids in peroxisomal disorders

      NEUROCHEMICAL RESEARCH
    67. Bakheet, S; Al-Essa, M; Patay, Z; Al-Watban, J; Dhaunsi, G; Powe, J; Ozand, PT
      Cerebral fluorine-18 fluorodeoxyglucose positron emission tomographic findings in X-linked adrenoleukodystrophy

      CLINICAL NUCLEAR MEDICINE
    68. Soule, S
      Addison's disease in Africa - a teaching hospital experience

      CLINICAL ENDOCRINOLOGY
    69. Maier, EM; Roscher, AA; Kammerer, S; Mehnert, K; Conzelmann, E; Holzinger, A
      Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical,immunocytochemical and DNA analyses

      PRENATAL DIAGNOSIS
    70. Garside, S; Rosebush, PI; Levinson, AJ; Mazurek, MF
      Late-onset adrenoleukodystrophy associated with long-standing psychiatric symptoms

      JOURNAL OF CLINICAL PSYCHIATRY
    71. Min, KT; Benzer, S
      Preventing neurodegeneration in the Drosophila mutant bubblegum

      SCIENCE
    72. Vion-Dury, J; Salvan, AM; Cozzone, PJ
      Proton magnetic resonance spectrometry for noninvasive exploration of human brain metabolism: current and future clinical applications.

      REVUE NEUROLOGIQUE
    73. Restuccia, D; Di Lazzaro, V; Valeriani, M; Oliviero, A; Le Pera, D; Barba, C; Cappa, M; Bertini, E; Di Capua, M; Tonali, P
      Neurophysiologic follow-up of long-term dietary treatment in adult-onset adrenoleukodystrophy

      NEUROLOGY
    74. Yamada, T; Taniwaki, T; Shinnoh, N; Uchiyama, A; Shimozawa, N; Ohyagi, Y; Asahara, H; Kira, J
      Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisome

      NEUROLOGY
    75. Poulos, A; Stockham, PC; Johnson, DW; Paton, BC; Beckman, K; Singh, H
      Metabolism of trideuterated iso-lignoceric acid in rats in vivo and in human fibroblasts in culture

      LIPIDS
    76. Gomez-Lira, M; Perusi, C; Mottes, M; Pignatti, PF; Uziel, G; Rizzuto, N; Salviati, A
      Two novel frameshift mutations in the adrenoleukodystrophy gene in Italianpatients

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    77. van Geel, BM; Assies, J; Haverkort, EB; Koelman, JHTM; Verbeeten, B; Wanders, RJA; Barth, PG
      Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo'soil"

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    78. Chang, CC; South, S; Warren, D; Jones, J; Moser, AB; Moser, HW; Gould, SJ
      Metabolic control of peroxisome abundance

      JOURNAL OF CELL SCIENCE
    79. Liu, LX; Janvier, K; Berteaux-Lecellier, V; Cartier, N; Benarous, R; Aubourg, P
      Homo- and heterodimerization of peroxisomal ATP-binding cassette half-transporters

      JOURNAL OF BIOLOGICAL CHEMISTRY
    80. Imanaka, T; Aihara, K; Takano, T; Yamashita, A; Sato, R; Suzuki, Y; Yokota, S; Osumi, T
      Characterization of the 70-kDa peroxisomal membrane protein, an ATP binding cassette transporter

      JOURNAL OF BIOLOGICAL CHEMISTRY
    81. Flavigny, E; Sanhaj, A; Aubourg, P; Cartier, N
      Retroviral-mediated adrenoleukodystrophy-related gene transfer corrects very long chain fatty acid metabolism in adrenoleukodystrophy fibroblasts: implications for therapy

      FEBS LETTERS
    82. Berger, J; Albet, S; Bentejac, M; Netik, A; Holzinger, A; Roscher, AA; Bugaut, M; Forss-Petter, S
      The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    83. PERICHON R; BOURRE JM; KELLY JF; ROTH GS
      THE ROLE OF PEROXISOMES IN AGING

      Cellular and molecular life sciences
    84. DECRAEMER D; VANDENBRANDEN C; FONTAINE M; VAMECQ J
      EFFECTS OF LORENZOS OIL ON PEROXISOMES IN HEALTHY MICE

      PROSTAGLANDINS & OTHER LIPID MEDIATORS
    85. KORENKE GC; KRASEMANN E; MEIER V; BEUCHE W; HUNNEMAN DH; HANEFELD E
      FIRST MISSENSE MUTATION (W679R) IN EXON-10 OF THE ADRENOLEUKODYSTROPHY GENE IN SIBLINGS WITH ADRENOMYELONEUROPATHY

      Human mutation
    86. DOERFLINGER N; MICLEA JM; LOPEZ J; CHOMIENNE C; BOUGNERES P; AUBOURG P; CARTIER N
      RETROVIRAL TRANSFER AND LONG-TERM EXPRESSION OF THE ADRENOLEUKODYSTROPHY GENE IN HUMAN CD34(+) CELLS

      Human gene therapy
    87. Broccardo, C; Troffer-Charlier, N; Savary, S; Mandel, JL; Chimini, G
      Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    88. WERNER H; JUNG M; KLUGMANN M; SEREDA M; GRIFFITHS IR; NAVE KA
      MOUSE MODELS OF MYELIN DISEASES

      Brain pathology
    89. POWERS JM; MOSER HW
      PEROXISOMOL DISORDERS - GENOTYPE, PHENOTYPE, MAJOR NEUROPATHOLOGIC LESIONS, AND PATHOGENESIS

      Brain pathology
    90. BRAITERMAN LT; ZHENG SQ; WATKINS PA; GERAGHTY MT; JOHNSON G; MCGUINNESS MC; MOSER AB; SMITH KD
      SUPPRESSION OF PEROXISOMAL MEMBRANE-PROTEIN DEFECTS BY PEROXISOMAL ATP BINDING CASSETTE (ABC) PROTEINS

      Human molecular genetics
    91. SCHLEMMER HP; MOCKEL R; MARCUS A; HENTSCHEL F; GOPEL C; BECKER G; KOPKE J; GUCKEL F; SCHMIDT MH; GEORGI M
      PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN ACUTE, JUVENILE ANOREXIA-NERVOSA

      PSYCHIATRY RESEARCH-NEUROIMAGING
    92. CARMANT L; DECARIE JC; FON E; SHEVELL MI
      TRANSIENT VISUAL SYMPTOMS AS THE INITIAL MANIFESTATION OF CHILDHOOD ADRENOLEUKODYSTROPHY

      Pediatric neurology
    93. SAKAKIBARA R; HATTORI T; FUKUTAKE T; MORI M; YAMANISHI T; YASUDA K
      MICTURITIONAL DISTURBANCE IN A PATIENT WITH ADRENOMYELONEUROPATHY (AMN)

      Neurourol. urodyn.
    94. Seedorf, U
      Peroxisomes in lipid metabolism

      JOURNAL OF CELLULAR BIOCHEMISTRY
    95. Aversa, A; Palleschi, S; Cruccu, G; Silvestroni, L; Isidori, A; Fabbri, A
      Rapid decline of fertility in a case of adrenoleukodystrophy

      HUMAN REPRODUCTION
    96. POUWELS PJW; KRUSE B; KORENKE GC; MAO X; HANEFELD FA; FRAHM J
      QUANTITATIVE PROTON MAGNETIC-RESONANCE SPECTROSCOPY OF CHILDHOOD ADRENOLEUKODYSTROPHY

      Neuropediatrics
    97. GARTNER J; BROSIUS U; OBIE C; WATKINS PA; VALLE D
      RESTORATION OF PEX2 PEROXISOME ASSEMBLY DEFECTS BY OVEREXPRESSION OF PMP70

      European journal of cell biology
    98. KIRK EPE; FLETCHER JM; SHARP P; CAREY B; POULOS A
      X-LINKED ADRENOLEUKODYSTROPHY - THE AUSTRALASIAN EXPERIENCE

      American journal of medical genetics
    99. OSAKA H; SEKIGUCHI H; INOUE K; IKUTA K; SAKAKIHARA Y; OKA A; ONISHI H; MIYAKAWA T; SUZUKI K; KIMURA S; KOSAKA K; MATSUYAMA S
      A NOVEL MUTATION FOUND IN AN ADRENOLEUKODYSTROPHY PATIENT WHO UNDERWENT BONE-MARROW TRANSPLANTATION

      Journal of inherited metabolic disease
    100. WILLIAMS GA; PEARL GS; POLLACK MA; ANDERSON RE
      ADRENOLEUKODYSTROPHY - UNUSUAL CLINICAL AND RADIOGRAPHIC MANIFESTATION

      Southern medical journal (Birmingham, Ala.)


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/08/20 alle ore 19:48:24