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La ricerca find articoli where soggetti phrase all words 'HYPOPLASIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 1500 riferimenti
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    1. Davey, MG; Hooper, SB; Cock, ML; Harding, R
      Stimulation of lung growth in fetuses with lung hypoplasia leads to altered postnatal lung structure in sheep

      PEDIATRIC PULMONOLOGY
    2. Bush, A
      Congenital lung disease: A plea for clear thinking and clear nomenclature

      PEDIATRIC PULMONOLOGY
    3. McCarthy, VP; Zimo, DA; Lucas, MA
      Airway in the oculo-auriculo-vertebral spectrum: Two cases and a review ofthe literature

      PEDIATRIC PULMONOLOGY
    4. Chinoy, MR; Chi, XL; Cilley, RE
      Down-regulation of regulatory proteins for differentiation and proliferation in murine fetal hypoplastic lungs: Altered mesenchymal-epithelial interactions

      PEDIATRIC PULMONOLOGY
    5. Sokol, GM; Fineberg, NS; Wright, LL; Ehrenkranz, RA
      Changes in arterial oxygen tension when weaning neonates from inhaled nitric oxide

      PEDIATRIC PULMONOLOGY
    6. Fabris, VE; Pato, MD; Belik, J
      Progressive lung and cardiac changes associated with pulmonary hypertension in the fetal rat

      PEDIATRIC PULMONOLOGY
    7. Piedboeuf, B
      Regulation of alveolar growth

      PEDIATRIC PULMONOLOGY
    8. Myers, LP; Krieg, AM; Pruett, SB
      Bacterial DNA does not increase serum corticosterone concentration or prevent increases induced by other stimuli

      INTERNATIONAL IMMUNOPHARMACOLOGY
    9. Dhooge, I; Lantsoght, B; Lemmerling, M; Vanzieleghem, B; Mortier, G
      Hearing loss as a presenting symptom of cleidocranial dysplasia

      OTOLOGY & NEUROTOLOGY
    10. Bamiou, DE; Worth, S; Phelps, P; Sirimanna, T; Rajput, K
      Eighth nerve aplasia and hypoplasia in cochlear implant candidates: The clinical perspective

      OTOLOGY & NEUROTOLOGY
    11. McElreavey, K; Cortes, LS
      X-Y translocations and sex differentiation

      SEMINARS IN REPRODUCTIVE MEDICINE
    12. Van den Veyver, IB
      Skewed X inactivation in X-linked disorders

      SEMINARS IN REPRODUCTIVE MEDICINE
    13. Recto, MR; Elbl, F; Austin, E
      Use of the new IntraStent for treatment of transverse arch hypoplasia/coarctation of the aorta

      CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
    14. Fanelli, F; Themmen, APN; Puett, D
      Lutropin receptor function: Insights from natural, engineered, and computer-simulated mutations

      IUBMB LIFE
    15. Mahieu-Caputo, D; Sonigo, P; Dommergues, M; Fournet, JC; Thalabard, JC; Abarca, C; Benachi, A; Brunelle, F; Dumez, Y
      Fetal lung volume measurement by magnetic resonance imaging in congenital diaphragmatic hernia

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    16. Barkovich, AJ; Kuzniecky, RI; Dobyns, WB
      Radiologic classification of malformations of cortical development

      CURRENT OPINION IN NEUROLOGY
    17. Soylu, H; Kutlu, NO; Sonmezgoz, E; Bukte, Y; Ozgen, U; Akinci, A
      Prune-belly syndrome and pulmonary hypoplasia: A potential cause of death

      PEDIATRICS INTERNATIONAL
    18. Maruyama, K; Koizumi, T
      Oromandibular-limb hypogenesis with pulmonary hypoplasia

      PEDIATRICS INTERNATIONAL
    19. Shibata, H; Ikeda, Y; Mukai, T; Morohashi, K; Kurihara, I; Ando, T; Suzuki, T; Kobayashi, S; Murai, M; Saito, I; Saruta, T
      Expression profiles of COUP-TF, DAX-1, and SF-1 in the human adrenal glandand adrenocortical tumors: Possible implications in steroidogenesis

      MOLECULAR GENETICS AND METABOLISM
    20. Gleeson, JG
      Neuronal migration disorders

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    21. Fischer, A
      Primary T-lymphocyte immunodeficiencies

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    22. Vulliamy, TJ; Knight, SW; Mason, PJ; Dokal, I
      Very short telomeres in the peripheral blood of patients with X-linked andautosomal dyskeratosis congenita

      BLOOD CELLS MOLECULES AND DISEASES
    23. Vulliamy, TJ; Knight, SW; Mason, PJ; Dokal, I
      Very short telomeres in the peripheral blood of patients with X-linked andautosomal dyskeratosis congenita

      BLOOD CELLS MOLECULES AND DISEASES
    24. Khabbaze, Y; Karayalcin, G; Paley, C; Shende, A; Valderrama, E; Lipton, JM
      Thrombocytopenia absent corpus callosum syndrome: Third case of a distinctclinical entity

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    25. Thebaud, B; Barlier-Mur, AM; Chailley-Heu, B; Henrion-Caude, A; Tibboel, D; Dinh-Xuan, AT; Bourbon, JR
      Restoring effects of vitamin A on surfactant synthesis in nitrofen-inducedcongenital diaphragmatic hernia in rats

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    26. Guatelli-Steinberg, D
      What can developmental defects of enamel reveal about physiological stressin nonhuman primates?

      EVOLUTIONARY ANTHROPOLOGY
    27. Phelan, JK; McCabe, ERB
      Mutations in NROB1 (DAX1) and NR5A1 (SF1) responsible for adrenal hypoplasia congenita

      HUMAN MUTATION
    28. Ikeda, Y; Takeda, Y; Shikayama, T; Mukai, T; Hisano, S; Morohashi, KI
      Comparative localization of Dax-1 and Ad4BP/SF-1 during development of thehypothalamic-pituitary-gonadal axis suggests their closely related and distinct functions

      DEVELOPMENTAL DYNAMICS
    29. Chapple, JR; Nunn, JH
      The oral health of children with clefts of the lip, palate, or both

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    30. Maruko, E; Hayes, C; Evans, CA; Padwa, B; Mulliken, JB
      Hypodontia in hemifacial microsomia

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    31. Nagashima, T; Murakami, M; Onigata, K; Morimura, T; Nagashima, K; Mori, M; Morikawa, A
      Novel inactivating missense mutations in the thyrotropin receptor gene in Japanese children with resistance to thyrotropin

      THYROID
    32. Bretones, P; Duprez, L; Parma, J; David, M; Vassart, G; Rodien, P
      A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene

      THYROID
    33. Stelnicki, EJ; Boyd, JB; Nott, RL; Barnavon, Y; Uecker, C; Henson, T
      Early treatment of severe mandibular hypoplasia with distraction mesenchymogenesis and bilateral free fibula flaps

      JOURNAL OF CRANIOFACIAL SURGERY
    34. Cohen, SR; Holmes, RE
      Internal Le Fort III distraction with biodegradable devices

      JOURNAL OF CRANIOFACIAL SURGERY
    35. Uemura, T; Hayashi, T; Satoh, K; Mitsukawa, N; Yoshikawa, A; Jinnnai, T; Hosaka, Y
      A case of improved obstructive sleep apnea by distraction osteogenesis formidface hypoplasia of an infantile Crouzon's syndrome

      JOURNAL OF CRANIOFACIAL SURGERY
    36. Levine, JC; Sanders, SP; Colan, SD; Jonas, RA; Spevak, PJ
      The risk of having additional obstructive lesions in neonatal coarctation of the aorta

      CARDIOLOGY IN THE YOUNG
    37. Besada, E; Fisher, JP
      Absent relative afferent pupillary defect in an asymptomatic case of lateral chiasmal syndrome from cerebral aneurysm

      OPTOMETRY AND VISION SCIENCE
    38. Rosenfeld, CS; Roberts, RM; Lubahn, DB
      Estrogen receptor- and aromatase-deficient mice provide insight into the roles of estrogen within the ovary and uterus

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    39. Acosta, JM; Thebaud, B; Castillo, C; Mailleux, A; Tefft, D; Wuenschell, C; Anderson, KD; Bourbon, J; Thiery, JP; Bellusci, S; Warburton, D
      Novel mechanisms in murine nitrofen-induced pulmonary hypoplasia: FGF-10 rescue in culture

      AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
    40. Haley, KJ; Sunday, ME; Osathanondh, R; Du, J; Vathanaprida, C; Karpitsky, VV; Krause, JE; Lilly, CM
      Developmental expression of neurokinin A and functional neurokinin-2 receptors in lung

      AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
    41. Stormon, MO; Dorney, SFA; Kamath, KR; O'Loughlin, EV; Gaskin, KJ
      The changing pattern of diagnosis of infantile cholestasis

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    42. Chernykh, VB; Kurilo, LF
      Genetic control of sexual differentiation in humans

      RUSSIAN JOURNAL OF GENETICS
    43. Vanlieferinghen, P; Borderon, C; Francannet, C; Gembara, P; Dechelotte, P
      Johanson-Blizzard syndrome. A new case with autopsy findings

      GENETIC COUNSELING
    44. De Wyels, JV; De Smet, L
      Cleft hand between the ring and small finger associated with thumb hypoplasia: A casus

      GENETIC COUNSELING
    45. Heiss, NS; Megarbane, A; Klauck, SM; Kreuz, FR; Makhoul, E; Majewski, F; Poustka, A
      One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC)

      GENETIC COUNSELING
    46. Aynaci, FM; Aynaci, O; Ahmetoglu, A; Celep, F
      Fuhrmann syndrome associated with cortical dysplasia

      GENETIC COUNSELING
    47. Becker, R; Stiemer, B; Neumann, L; Entezami, M
      Mild ventriculomegaly, mild cerebellar hypoplasia and dysplastic choroid plexus as early prenatal signs of CHARGE association

      FETAL DIAGNOSIS AND THERAPY
    48. Laberge, JM; Flageole, H; Pugash, D; Khalife, S; Blair, G; Filiatrault, D; Russo, P; Lees, G; Wilson, RD
      Outcome of the prenatally diagnosed congenital cystic adenomatoid lung malformation: A Canadian experience

      FETAL DIAGNOSIS AND THERAPY
    49. Erez, E; Tam, VKH; Williams, WH; Kanter, KR
      The Konno aortoventriculoplasty for repeat aortic valve replacement

      EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY
    50. Priston, M; Kozlowski, K; Gill, D; Letwin, K; Buys, Y; Levin, AV; Walter, MA; Heon, E
      Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome

      HUMAN MOLECULAR GENETICS
    51. de Ravel, TJL; Legius, E; Brems, H; Van Hoestenberghe, R; Gillis, P; Fryns, JP
      Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor

      CLINICAL DYSMORPHOLOGY
    52. Megarbane, A
      A new familial syndrome with facial abnormalities, abnormal EEG, and mental retardation

      CLINICAL DYSMORPHOLOGY
    53. Spranger, J; Self, S; Clarkson, KB; Pai, GS
      Ischiospinal dysostosis with rib gaps and nephroblastomatosis

      CLINICAL DYSMORPHOLOGY
    54. Verloes, A; Lesenfants, S
      New syndrome: clavicle hypoplasia, facial dysmorphism, severe myopia, single central incisor and peripheral neuropathy

      CLINICAL DYSMORPHOLOGY
    55. Tobias, ES; Patrick, WJA; MacKenzie, JR; Whiteford, ML
      A case of Acro-renal-mandibular syndrome in an 18 week male fetus

      CLINICAL DYSMORPHOLOGY
    56. Tanemura, M; Nishikawa, N; Kojima, K; Suzuki, Y; Suzumori, K
      A case of successful fetal therapy for congenital chylothorax by intrapleural injection of OK-432

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    57. Mulder, EJH; Nikkels, PGJ; Visser, GHA
      Fetal akinesia deformation sequence: behavioral development in a case of congenital myopathy

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    58. Paladini, D; Tartaglione, A; Agangi, A; Foglia, S; Martinelli, P; Nappi, C
      Pena-Shokeir phenotype with variable onset in three consecutive pregnancies

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    59. Babita, G; Rashmi, M; Deb, K
      Combined spinal epidural anesthesia for cesarean section in a patient withleft lung agenesis

      INTERNATIONAL JOURNAL OF OBSTETRIC ANESTHESIA
    60. Lines, A; Gillett, AM; Phillips, ID; Wallace, MJ; Hooper, SB
      Re-expression of pulmonary surfactant proteins following tracheal obstruction in fetal sheep

      EXPERIMENTAL PHYSIOLOGY
    61. Connor, SEJ; Chandler, C; Robinson, S; Jarosz, JM
      Congenital midline cleft of the posterior arch of atlas: a rare cause of symptomatic cervical canal stenosis

      EUROPEAN RADIOLOGY
    62. Blinder, G; Corat-Simon, J; Hershkovitz, E
      Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disorders

      EUROPEAN RADIOLOGY
    63. Apostolou, T; Nikolopoulou, N; Theodoridis, M; Kournoustiotis, V; Pavlopoulou, E; Chondros, D; Billis, A
      Late onset of renal disease in nephronophthisis with features of Joubert syndrome type B

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    64. Rodriguez-Soriano, J; Vallo, A; Bilbao, JR; Castano, L
      Branchio-oto-renal syndrome: identification of a novel mutation in the EYA1 gene

      PEDIATRIC NEPHROLOGY
    65. Smolkin, V; Halevy, R; Koren, A
      Steroid responsive nephrotic syndrome associated with bilateral renal dysplasia

      PEDIATRIC NEPHROLOGY
    66. Saigusa, K; Aoki, Y; Horiguchi, M
      Hypoplasia of the left lobe of the liver

      SURGICAL AND RADIOLOGIC ANATOMY
    67. Tamura, M; Kanno, Y; Chuma, S; Saito, T; Nakatsuji, N
      Pod-1/Capsulin shows a sex- and stage-dependent expression pattern in the mouse gonad development and represses expression of Ad4BP/SF-1

      MECHANISMS OF DEVELOPMENT
    68. Jalevik, B; Noren, JG; Klingberg, G; Barregard, L
      Etiologic factors influencing the prevalence of demarcated opacities in permanent first molars in a group of Swedish children

      EUROPEAN JOURNAL OF ORAL SCIENCES
    69. Hardan, AY; Minshew, NJ; Harenski, K; Keshavan, MS
      Posterior fossa magnetic resonance imaging in autism

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    70. Aigueperse, C; Val, P; Pacot, C; Darne, C; Lalli, E; Sassone-Corsi, P; Veyssiere, G; Jean, C; Martinez, A
      SF-1 (steroidogenic factor-1), C/EBP beta (CCAAT/enhancer binding protein), and ubiquitous transcription factors NF1 (nuclear factor 1) and Sp1 (selective promoter factor 1) are required for regulation of the mouse aldose reductase-like gene (AKR1B7) expression in adrenocortical cells

      MOLECULAR ENDOCRINOLOGY
    71. Hishinuma, A; Ohyama, Y; Kuribayashi, T; Nagakubo, N; Namatame, T; Shibayama, K; Arisaka, O; Matsuura, N; Ieiri, T
      Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    72. Ambrugger, P; Stoeva, I; Biebermann, H; Torresani, T; Leitner, C; Gruters, A
      Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    73. Makitie, OM; Tapanainen, PJ; Dunkel, L; Siimes, MA
      Impaired spermatogenesis: an unrecognized feature of cartilage-hair hypoplasia

      ANNALS OF MEDICINE
    74. Trevisan, CP; Pastorello, E; Tonello, S; Armani, M; Rigoni, MT; Tormene, AP; Freda, MP; Zortea, M; Lombardi, S
      Ataxia and Congenital Muscular Dystrophy: the follow-up of a new specific phenotype

      BRAIN & DEVELOPMENT
    75. Takahashi, J; Fukuda, T; Tanaka, J; Minamitani, M; Onouchi, K; Makioka, A
      Bax-induced apoptosis not demonstrated in the congenital toxoplasmosis in mice

      BRAIN & DEVELOPMENT
    76. Bajanowski, T; Rossi, L; Biondo, B; Ortmann, C; Haverkamp, W; Wedekind, H; Jorch, G; Brinkmann, B
      Prolonged QT interval and sudden infant death - report of two cases

      FORENSIC SCIENCE INTERNATIONAL
    77. Yamakawa, M; Furuuchi, S
      Expression and antigenic characterization of the major core protein VP7 ofChuzan virus, a member of the Palyam serogroup orbiviruses

      VETERINARY MICROBIOLOGY
    78. Scharnhorst, V; van der Eb, AJ; Jochemsen, AG
      WT1 proteins: functions in growth and differentiation

      GENE
    79. Martinez-Lazaro, R; Cortes-Blanco, A; Banzo, J
      Global absence of pulmonary perfusion in a hypoplastic lung with pulmonaryartery agenesis associated with immunoglobulin A deficit

      CLINICAL NUCLEAR MEDICINE
    80. Breier, DV; Rendo, P; Gonzalez, J; Shilton, G; Stivel, M; Goldztein, S
      Massive plasmocytosis due to methimazole-induced bone marrow toxicity

      AMERICAN JOURNAL OF HEMATOLOGY
    81. Endo, A; Minato, M; Takada, M; Takahashi, S; Harada, K; Yamada, T; Takashima, S
      A case of pulmonary hypoplasia associated with intrauterine brainstem necrosis

      EUROPEAN JOURNAL OF PEDIATRICS
    82. Fokstuen, S; Vrticka, K; Riegel, M; Da Silva, V; Baumer, A; Schinzel, A
      Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial(Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2

      EUROPEAN JOURNAL OF PEDIATRICS
    83. Wiltshire, E; Couper, J; Rodda, C; Jameson, JL; Achermann, JC
      Variable presentation of X-linked adrenal hypoplasia congenita

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    84. Achermann, JC; Jameson, JL
      Advances in the molecular genetics of hypogonadotropic hypogonadism

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    85. Golden, JA
      Cell migration and cerebral cortical development

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    86. Veitia, RA; Salas-Cortes, L; Ottolenghi, C; Pailhoux, E; Cotinot, C; Fellous, M
      Testis determination in mammals: more questions than answers

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    87. Achermann, JC; Weiss, J; Lee, EJ; Jameson, JL
      Inherited disorders of the gonadotropin hormones

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    88. Stocco, DM; Clark, BJ; Reinhart, AJ; Williams, SC; Dyson, M; Dassi, B; Walsh, LP; Manna, PR; Wang, XJ; Zeleznik, AJ; Orly, J
      Elements involved in the regulation of the StAR gene

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    89. Smith, SP; Bunker, TD
      Primary glenoid dysplasia - A review of 12 patients

      JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME
    90. Laudy, JAM
      Doppler ultrasonography of the human fetal pulmonary circulation

      EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
    91. Goasdoue, P; Rodriguez, D; Moutard, ML; Robain, O; Lalande, G; Adamsbaum, C
      Pontoneocerebellar hypoplasia: definition of MR features

      PEDIATRIC RADIOLOGY
    92. Rosendahl, K; Maurseth, K; Olsen, OE; Halvorsen, OJ; Gjelland, K; Engebretsen, L
      Neonatal lethal dwarfism with distinct skeletal malformations - a separateentity?

      PEDIATRIC RADIOLOGY
    93. Graham, JM; Krakow, D; Tolo, VT; Smith, AK; Lachman, RS
      Radiographic findings and Gs-alpha bioactivity studies and mutation screening in acrodysostosis indicate a different etiology from pseudohypoparathyroidism

      PEDIATRIC RADIOLOGY
    94. Quinton, R; Duke, VM; Robertson, A; Kirk, JMW; Matfin, G; de Zoysa, PA; Azcona, C; MacColl, GS; Jacobs, HS; Conway, GS; Besser, M; Stanhope, RG; Bouloux, PMG
      Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

      CLINICAL ENDOCRINOLOGY
    95. Salvatori, R; Fan, XG; Phillips, JA; Prince, M; Levine, MA
      Isolated growth hormone (GH) deficiency due to compound heterozygosity fortwo new mutations in the GH-releasing hormone receptor gene

      CLINICAL ENDOCRINOLOGY
    96. Eggesbo, HB; Sovik, S; Dolvik, S; Eiklid, K; Kolmannskog, F
      CT characterization of developmental variations of the paranasal sinuses in cystic fibrosis

      ACTA RADIOLOGICA
    97. Platzbecker, U; Thiede, C; Freiberg-Richter, J; Rollig, C; Helwig, A; Schakel, U; Mohr, B; Schaich, M; Ehninger, G; Bornhauser, M
      Early allogeneic blood stem cell transplantation after modified conditioning therapy during marrow aplasia: stable remission in high-risk acute myeloid leukemia

      BONE MARROW TRANSPLANTATION
    98. Boltshauser, E
      Cerebellar imaging - an important signpost in paediatric neurology

      CHILDS NERVOUS SYSTEM
    99. Heling, KS; Tennstedt, C; Chaoui, R; Kalache, KD; Hartung, J; Bollmann, R
      Reliability of prenatal sonographic lung biometry in the diagnosis of pulmonary hypoplasia

      PRENATAL DIAGNOSIS
    100. Roberts, A
      Prenatal diagnosis of pulmonary hypoplasia

      PRENATAL DIAGNOSIS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 07/06/20 alle ore 00:00:10