Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words 'TADINI G' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 52 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Gualandri, L; Cambiaghi, S; Ermacora, E; Tadini, G; Gianotti, R; Caputo, R
      Multiple familial smooth muscle hamartomas

      PEDIATRIC DERMATOLOGY
    2. Gardella, R; Nuytinck, L; Barlati, S; Van Acker, P; Tadini, G; De Paepe, A; Colombi, M
      Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    3. Fine, JD; Eady, RAJ; Bauer, EA; Briggaman, RA; Bruckner-Tuderman, L; Christiano, A; Heagerty, A; Hintner, H; Jonkman, MF; McGrath, J; McGuire, J; Moshell, A; Shimizu, H; Tadini, G; Uitto, J
      Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    4. Restano, L; Cambiaghi, S; Brusasco, A; Tadini, G; Caputo, R
      A hyperkeratotic linear lesion in a girl with KID syndrome. A further example of early allelic loss?

      EUROPEAN JOURNAL OF DERMATOLOGY
    5. Gardella, R; Zoppi, N; Ferraboli, S; Marini, D; Tadini, G; Barlati, S; Colombi, M
      Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: Analysis of transcript levels in dermal fibroblasts

      HUMAN MUTATION
    6. Restano, L; Cambiaghi, S; Tadini, G
      The pattern of inheritance in KID syndrome

      PEDIATRIC DERMATOLOGY
    7. Cambiaghi, S; Restano, L; Tadini, G
      Atrophoderma vermiculata along Blaschko lines

      PEDIATRIC DERMATOLOGY
    8. VERALDI S; GORANI A; SUSS L; TADINI G
      CUTANEOUS MYIASIS CAUSED BY DERMATOBIA-HOMINIS

      Pediatric dermatology
    9. Restano, L; Cambiaghi, S; Tadini, G; Cerri, A; Caputo, R
      Blaschko lines of the face: A step closer to completing the map

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    10. TADINI G; GARDELLA R; ZOPPI N; FERRABOLL S; BARLATI S; COLOMBI M
      MOLECULAR CHARACTERIZATION OF 2 PATIENTS AFFECTED BY THE HALLOPEAU-SIEMENS VARIANT OF RECESSIVE EPIDERMOLYSIS-BULLOSA DYSTROPHICA

      Journal of investigative dermatology
    11. CAMBIAGHI S; PISTRITTO G; TADINI G; GELMETTI C
      HAIRY ELBOWS

      International journal of dermatology
    12. BRUSASCO A; CAMBIAGHI S; TADINI G; BERTI E; CAPUTO R
      UNUSUAL HYPERPIGMENTATION DEVELOPING IN CONGENITAL RETICULAR ICHTHYOSIFORM ERYTHRODERMA (ICHTHYOSIS VARIEGATA)

      British journal of dermatology
    13. BRUSASCO A; VERALDI S; TADINI G; CAPUTO R
      LOCALIZED PEELING SKIN SYNDROME - CASE-REPORT WITH ULTRASTRUCTURAL-STUDY

      British journal of dermatology
    14. TADINI G; RESTANO L; GONZALESPEREZ R; GONZALESENSENAT A; VINCENTEVILLA MA; CAMBIAGHI S; MARCHETTINI P; MASTRANGELO M; HAPPLE R
      PHAKOMATOSIS PIGMENTOKERATOTICA - REPORT OF NEW CASES AND FURTHER DELINEATION OF THE SYNDROME

      Archives of dermatology
    15. CAVALLI R; RESTANO L; CAMBIAGHI S; TADINI G
      OMENN SYNDROME - A CASE-REPORT OF A SUCCESSFUL, HETEROLOGOUS BONE-MARROW TRANSPLANTATION

      EJD. European journal of dermatology
    16. CAMBIAGHI S; BRUSASCO A; RESTANO L; CAVALLI R; TADINI G
      EPIDERMOLYSIS-BULLOSA PRURIGINOSA

      Dermatology
    17. BARBARESCHI M; CAMBIAGHI S; CRUPI AC; TADINI G
      FAMILY WITH PURE HAIR-NAIL ECTODERMAL DYSPLASIA

      American journal of medical genetics
    18. CHAVANAS S; TADINI G
      A HOMOZYGOUS IN-FRAME DELETION IN THE COLLAGENOUS DOMAIN OF BULLOUS PEMPHIGOID ANTIGEN BP180 (TYPE-XVII COLLAGEN) CAUSES GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA (VOL 109, PG 74, 1997)

      Journal of investigative dermatology
    19. CHAVANAS S; GACHE Y; TADINI G; PULKKINEN L; UITTO J; ORTONNE JP; MENEGUZZI G
      A HOMOZYGOUS IN-FRAME DELETION IN THE COLLAGENOUS DOMAIN OF BULLOUS PEMPHIGOID ANTIGEN BP180 (TYPE-XVII COLLAGEN) CAUSES GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA

      Journal of investigative dermatology
    20. BROWN TA; GIL SG; SYBERT VP; LESTRINGANT GG; TADINI G; CAPUTO R; CARTER WG
      DEFECTIVE INTEGRIN ALPHA-6-BETA-4 EXPRESSION IN THE SKIN OF PATIENTS WITH JUNCTIONAL EPIDERMOLYSIS-BULLOSA AND PYLORIC ATRESIA (VOL 107, PG354, 1996)

      Journal of investigative dermatology
    21. BRUSASCO A; GELMETTI C; TADINI G; CAPUTO R
      ICHTHYOSIS CONGENITA TYPE-IV - A NEW CASE RESEMBLING DIFFUSE CUTANEOUS MASTOCYTOSIS

      British journal of dermatology
    22. BRUSASCO A; RESTANO L; CAMBIAGHI S; TADINI G
      THE TYPICAL TIGER TAIL PATTERN OF THE HAIR SHAFT IN TRICHOTHIODYSTROPHY MAY NOT BE EVIDENT AT BIRTH

      Archives of dermatology
    23. BRUSASCO A; RESTANO L; CAMBIAGHI S; TADINI G
      TIGER TAIL PATTERN ON POLARIZED HAIR MICROSCOPIC EXAMINATION IS FOUNDIN HEALTHY INFANTS - REPLY

      Archives of dermatology
    24. HAPPLE R; HOFFMANN R; RESTANO L; CAPUTO R; TADINI G
      PHAKOMATOSIS PIGMENTOKERATOTICA - A MELANOCYTIC-EPIDERMAL TWIN NEVUS SYNDROME

      American journal of medical genetics
    25. TADINI G; BRUSASCO A; CAMBIAGHI S; CAVALLI R; CAPUTO R
      DYSTROPHIC EPIDERMOLYSIS-BULLOSA WITH PRURIGO-LIKE LESIONS - AN ULTRASTRUCTURAL-STUDY AND A PATHOGENETIC HYPOTHESIS

      Journal of investigative dermatology
    26. TADINI G; RESTANO L; HOFFMANN R; HAPPLE R
      MELANOCYTIC-EPIDERMAL TWIN NEVUS SYNDROME (PHACHOMATOSIS-PIGMENTOKERATOTICA) - A RECENTLY RECOGNIZED ECTODERMAL MOSAICISM

      Journal of investigative dermatology
    27. BRUSASCO A; VERALDI S; TADINI G; CAPUTO R
      LOCALIZED CONTINUOUS PEELING SKIN SYNDROME

      Journal of investigative dermatology
    28. TADINI G; CAVALLI R; BRUSASCO A; CAMBIAGHI S; ORTONNE JP; MENEGUZZI G
      A NEW SUBSET OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA IS CHARACTERIZED BY THE ABUSE OF IMMUNOREACTIVITY OF THE ANCHORING FILAMENT PROTEIN LADININ-1

      Journal of investigative dermatology
    29. BROWN TA; GIL SG; SYBERT VP; LESTRINGANT GG; TADINI G; CAPUTO R; CARTER WG
      DEFECTIVE INTEGRIN ALPHA-6-BETA-4 EXPRESSION IN THE SKIN OF PATIENTS WITH JUNCTIONAL EPIDERMOLYSIS-BULLOSA AND PYLORIC ATRESIA

      Journal of investigative dermatology
    30. BRUSASCO A; CAMOZZI S; RESTANO L; TADINI G
      ICHTHYOSIS CONGENITA TYPE-III - REPORT OF A CASE MISDIAGNOSED AS EPIDERMOLYTIC HYPERKERATOSIS

      Journal of investigative dermatology
    31. SCHMITT EC; CAMOZZI S; VIGO G; TADINI G
      TINEA-CORPORIS RESEMBLING DERMATOPHYTE COLONIES ON SABOURAUDS AGAR INA PATIENT WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS

      Archives of dermatology
    32. TADINI G; ERMACORA E; CARMINATI G; GELMETTI C; CAMBIAGHI S; BRUSASCO A; CAPUTO R; HAPPLE R
      UNILATERAL SPECKLED-LENTIGINOUS NEVUS, CONTRALATERAL VERRUCOUS EPIDERMAL NEVUS, AND DIFFUSE ICHTHYOSIS-LIKE HYPERKERATOSIS - AN UNUSUAL EXAMPLE OF TWIN SPOTTING

      EJD. European journal of dermatology
    33. TADINI G; KANITAKIS J; CAVALLI R; SCHMITT D; CAMBIAGHI S; BERTI E
      ALTERED EXPRESSION OF A NEW ANTIGEN OF THE DERMAL-EPIDERMAL JUNCTION (NU-T2 DEJ AG) IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA

      Archives of dermatological research
    34. TADINI G; BROWN TA; SYBERT VP; LESTRINGANT GG; CAVALLI R; BRUSASCO A; CARTER WG
      ABSENCE OF EXPRESSION OF THE ALPHA-6-BETA-4 INTEGRIN DEFINES THE PATIENTS WITH JUNCTIONAL EPIDERMOLYSIS BULLOSA-PYLORIC ATRESIA SUBSET

      Journal of investigative dermatology
    35. VIDAL F; TADINI G; GALLIANO MF; CAMBIAGHI S; MENEGUZZI G; ORTONNE IP
      MOLECULAR ANALYSIS FOR A PRENATAL-DIAGNOSIS USING CHORIONIC VILLI SAMPLES IN A FAMILY WITH RISK FOR RECURRENCE OF HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA

      Journal of investigative dermatology
    36. CAMBIAGHI S; TADINI G; BARBARESCHI M; CAPUTO R
      OLMSTED SYNDROME IN TWINS

      Archives of dermatology
    37. BRUSASCO A; TADINI G; CAMBIAGHI S; ERMACORA E; GRIMALT R; CAPUTO R
      A CASE OF CONGENITAL RETICULAR ICHTHYOSIFORM ERYTHRODERMA - ICHTHYOSIS EN CONFETTIS

      Dermatology
    38. BAUDOIN C; MIQUEL C; GAGNOUXPALACIOS L; PULKKINEN L; CHRISTIANO AM; UITTO J; TADINI G; ORTONNE JP; MENEGUZZI G
      A NOVEL HOMOZYGOUS NONSENSE MUTATION IN THE LAMC2 GENE IN PATIENTS WITH THE HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA

      Human molecular genetics
    39. GRIMALT R; GELMETTI C; BRUSASCO A; TADINI G; CAPUTO R
      PITYRIASIS ROTUNDA - REPORT OF A FAMILIAL OCCURRENCE AND REVIEW OF THE LITERATURE

      Journal of the American Academy of Dermatology
    40. GRIMALT R; GELMETTI C; BRUSASCO A; TADINI G; CAPUTO R
      PITYRIASIS ROTUNDA - REPORT OF A FAMILIAL OCCURRENCE AND REVIEW OF THE LITERATURE

      Journal of the American Academy of Dermatology
    41. PALLER AS; SYDER AJ; CHAN YM; HUTTON E; TADINI G; FUCHS E
      GENETIC AND CLINICAL MOSAICISM IN A TYPE OF EPIDERMAL NEVUS

      The New England journal of medicine
    42. GALLIANO MF; BAUDOIN C; TADINI G; CAVALLI R; BRUSASCO A; MENEGUZZI G; ORTONNE JP
      FURTHER EVIDENCE THAT IMPAIRED EXPRESSION OF LAMC2 GENE IS INVOLVED IN THE HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA

      Journal of investigative dermatology
    43. PALLER AS; SYDER AJ; CHAN YM; YU QC; HUTTON E; TADINI G; FUCHS E
      KERATIN GENE MOSAICISM IS THE GENETIC-BASIS FOR EPIDERMAL NEVUS, EPIDERMOLYTIC HYPERKERATOSIS TYPE

      Journal of investigative dermatology
    44. TADINI G; NALDI L; LOCATI L; CAMOZZI S; CAINELLI T
      EPIDEMIOLOGIC SURVEY ON EPIDERMOLYSIS-BULLOSA IN ITALY - FORMATION OFA NATIONAL REGISTRY

      Journal of investigative dermatology
    45. TADINI G; KANITAKIS J; CAVALLI R; CAMBIAGHI S; SCHMITT D; BERTI E
      ALTERED EXPRESSION OF A NEW ANTIGEN OF THE DERMAL-EPIDERMAL JUNCTION (NU-T2 DEJ AG) IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA

      Journal of investigative dermatology
    46. BAUDOIN C; TADINI G; GALLIANO F; CAVALLI R; BRUSASCO A; MENEGUZZI G; ORTONNE JP
      IDENTIFICATION OF A NOVEL HOMOZYGOUS NONSENSE MUTATION IN THE LAM C2 GENE IN A FAMILY AFFECTED BY HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA

      Journal of investigative dermatology
    47. BRUSASCO A; CAMBIAGHI S; TADINI G; MARINONI S; CAPUTO R
      ICHTHYOSIS CONGENITA IN TRICHOTHIODYSTROPHY ASSOCIATED WITH GROUP-D XERODERMA-PIGMENTOSUM - ULTRASTRUCTURAL-STUDY OF 5 CASES

      Journal of investigative dermatology
    48. CAMBIAGHI S; TADINI G; BARBARESCHI M; MENNI S; CAPUTO R
      RAPP-HODGKIN SYNDROME AND AEC SYNDROME - ARE THEY THE SAME ENTITY

      British journal of dermatology
    49. BRUSASCO A; CAVALLI R; CAMBIAGHI S; TADINI G; BERTI E; CAPUTO R
      ICHTHYOSIS CURTH-MACKLIN - A NEW SPORADIC CASE WITH IMMUNOHISTOCHEMICAL STUDY OF KERATIN EXPRESSION

      Archives of dermatology
    50. CAMBIAGHI S; TADINI G
      A NEW SYNDROME

      Pediatric dermatology
    51. TADINI G; CAMBIAGHI S; SCARABELLI G; BRUSASCO A; VIGO P
      FAMILIAL OCCURRENCE OF ISOLATED ACCESSORY TRAGI

      Pediatric dermatology
    52. TURCO AE; PEISSEL B; ROSSETTI S; SELICORNI A; MANOUKIAN S; BRUSASCO A; TADINI G; GALIMBERTI A; TASSIS B; TUROLLA L; TENCONI R; PIGNATTI PF
      PRENATAL TESTING IN A FETUS AT RISK FOR AUTOSOMAL-DOMINANT POLYCYSTICKIDNEY-DISEASE AND AUTOSOMAL RECESSIVE JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA

      American journal of medical genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/01/21 alle ore 06:38:11