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La ricerca find articoli where soggetti phrase all words 'PARTIAL LIPODYSTROPHY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 63 riferimenti
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    1. Hegele, RA
      Molecular basis of partial lipodystrophy and prospects for therapy

      TRENDS IN MOLECULAR MEDICINE
    2. Burke, B; Mounkes, LC; Stewart, C
      The nuclear envelope in muscular dystrophy and cardiovascular diseases

      TRAFFIC
    3. Weyer, C; Wolford, JK; Hanson, RL; Foley, JE; Tataranni, PA; Bogardus, C; Pratley, RE
      Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21-q23 and is associated with a common polymorphism in LMNA in Pima Indians

      MOLECULAR GENETICS AND METABOLISM
    4. Jakobs, PM; Hanson, EL; Crispell, KA; Toy, W; Keegan, H; Schilling, K; Icenogle, TB; Litt, M; Hershberger, RE
      Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

      JOURNAL OF CARDIAC FAILURE
    5. Mounkes, LC; Burke, B; Stewart, CL
      The A-type lamins - Nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases

      TRENDS IN CARDIOVASCULAR MEDICINE
    6. Holt, I; Clements, L; Manilal, S; Brown, SC; Morris, GE
      The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. Kitaguchi, T; Matsubara, S; Sato, M; Miyamoto, K; Hirai, S; Schwartz, K; Bonne, G
      A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block

      NEUROMUSCULAR DISORDERS
    8. Zietz, B; Barth, N; Scholmerich, J; Schmitz, G; Schaffler, A
      Gly15Gly polymorphism within the human adipocyte-specific apM-1gene but not Tyr111His polymorphism is associated with higher levels of cholesterol and LDL-cholesterol in caucasian patients with type 2 diabetes

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    9. Bulbul, M; Erdogan, O; Demircin, G; Altuntas, B; Memis, L; Oner, AE
      Acute pancreatitis in a patient with partial lipodystrophy and membranoproliferative glomerulonephritis

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    10. Salina, D; Bodoor, K; Enarson, P; Raharjo, WH; Burke, B
      Nuclear envelope dynamics

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    11. Sewry, CA; Brown, SC; Mercuri, E; Bonne, G; Feng, L; Camici, G; Morris, GE; Muntoni, F
      Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    12. Kazlauskaite, R; Santomauro, AT; Goldman, J; Silver, K; Snitker, S; Beamer, BA; Yen, CJ; Shuldiner, AR; Wajchenberg, BL
      A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. Lack of association of CGL with polymorphism in the laminA/C Gene

      CLINICAL ENDOCRINOLOGY
    13. Heydemann, A; Wheeler, MT; McNally, EM
      Cardiomyopathy in animal models of muscular dystrophy

      CURRENT OPINION IN CARDIOLOGY
    14. Brown, CA; Lanning, RW; McKinney, KQ; Salvino, AR; Cherniske, E; Crowe, CA; Darras, BT; Gominak, S; Greenberg, CR; Grosmann, C; Heydemann, P; Mendell, JR; Pober, BR; Sasaki, T; Shapiro, F; Simpson, DA; Suchowersky, O; Spence, JE
      Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifussmuscular dystrophy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Frayn, KN
      Adipose tissue and the insulin resistance syndrome

      PROCEEDINGS OF THE NUTRITION SOCIETY
    16. Ku, NO; Gish, R; Wright, TL; Omary, MB
      Keratin 8 mutations in patients with cryptogenic liver disease.

      NEW ENGLAND JOURNAL OF MEDICINE
    17. Paglione, AM; Ferrari, N; Berg, G; Frechtel, G; Taverna, M; Fasulo, V; Lopez, GI; Gomez, RM; Bruno, O; Ruiz, M; Wikinski, RLW
      Acquired partial lipodystrophy. Insulin resistance, hepatic lipase activity and small and dense LDL particles.

      MEDICINA-BUENOS AIRES
    18. Nadler, ST; Attie, AD
      Please pass the chips: Genomic insights into obesity and diabetes

      JOURNAL OF NUTRITION
    19. Hegele, RA; Huff, MW; Young, TK
      Common genomic variation in LMNA modulates indexes of obesity in Inuit

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    20. Muralikrishna, B; Dhawan, J; Rangaraj, N; Parnaik, VK
      Distinct changes in intranuclear lamin A/C organization during myoblast differentiation

      JOURNAL OF CELL SCIENCE
    21. Nili, E; Cojocaru, GS; Kalma, Y; Ginsberg, D; Copeland, NG; Gilbert, DJ; Jenkns, NA; Berger, R; Shaklai, S; Amariglio, N; Brok-Simoni, F; Simon, AJ; Rechavi, G
      Nuclear membrane protein LAP2 beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less)

      JOURNAL OF CELL SCIENCE
    22. Vaughan, OA; Alvarez-Reyes, M; Bridger, JM; Broers, JLV; Ramaekers, FCS; Wehnert, M; Morris, GE; Whitfield, WGF; Hutchison, CJ
      Both emerin and lamin C depend on lamin A for localization at the nuclear envelope

      JOURNAL OF CELL SCIENCE
    23. Hutchison, CJ; Alvarez-Reyes, M; Vaughan, OA
      Lamins in disease: why do ubiquitously expressed nuclear envelope proteinsgive rise to tissue-specific disease phenotypes?

      JOURNAL OF CELL SCIENCE
    24. Wolford, JK; Hanson, RL; Bogardus, C; Prochazka, M
      Analysis of the Lamin A/C gene as a candidate for Type II diabetes susceptibility in Pima Indians

      DIABETOLOGIA
    25. Caron, M; Auclair, R; Vigouroux, C; Glorian, M; Forest, C; Capeau, J
      The HIV protease inhibitor indinavir impairs sterol regulatory element-binding protein-1 intranuclear localization, inhibits preadipocyte differentiation, and induces insulin resistance

      DIABETES
    26. Ebihara, K; Ogawa, Y; Masuzaki, H; Shintani, M; Miyanaga, F; Aizawa-Abe, M; Hayashi, T; Hosoda, K; Inoue, G; Yoshimasa, Y; Gavrilova, O; Reitman, ML; Nakao, K
      Transgenic overexpression of leptin rescues insulin resistance and diabetes in a mouse model of lipoatrophic diabetes

      DIABETES
    27. Busch, CP; Hegele, RA
      Genetic determinants of type 2 diabetes mellitus

      CLINICAL GENETICS
    28. Brodsky, GL; Mestroni, L; Muntoni, F; Sewry, C; Miocic, S; Sinagra, G
      Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement - Response

      CIRCULATION
    29. Schmidt, HHJ; Lochs, H
      Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement

      CIRCULATION
    30. Hegele, RA
      Premature atherosclerosis associated with monogenic insulin resistance

      CIRCULATION
    31. Schonberger, J; Seidman, CE
      Many roads lead to a broken heart: The genetics of dilated cardiomyopathy

      AMERICAN JOURNAL OF HUMAN GENETICS
    32. Nagano, A; Arahata, K
      Nuclear envelope proteins acid associated diseases

      CURRENT OPINION IN NEUROLOGY
    33. Hegele, RA; Cao, HN; Harris, SB; Zinman, B; Hanley, AJ; Anderson, CM
      Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians

      PHYSIOLOGICAL GENOMICS
    34. Hegele, RA; Anderson, CM; Wang, J; Jones, DC; Cao, HN
      Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes

      GENOME RESEARCH
    35. Steel, KP
      A take on the tectorial membrane

      NATURE GENETICS
    36. Shackleton, S; Lloyd, DJ; Jackson, SNJ; Evans, R; Niermeijer, MF; Singh, BM; Schmidt, H; Brabant, G; Kumar, S; Durrington, PN; Gregory, S; O'Rahilly, S; Trembath, RC
      LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

      NATURE GENETICS
    37. Genschel, J; Schmidt, HHJ
      Mutations in the LMNA gene encoding lamin A/C

      HUMAN MUTATION
    38. Emery, AEH
      Emery-Dreifuss muscular dystrophy - a 40 year retrospective

      NEUROMUSCULAR DISORDERS
    39. Bogdanovic, RM; Dimitrijevic, JZ; Nikolic, VN; Ognjanovic, MV; Rodic, BD; Slavkovic, BV
      Membranoproliferative glomerulonephritis in two siblings: report and literature review

      PEDIATRIC NEPHROLOGY
    40. Hegele, RA; Anderson, CM; Cao, HN
      Lamin A/C mutation in a woman and her two daughters with Dunnigan-type partial lipodystrophy and insulin resistance

      DIABETES CARE
    41. Guelinckx, PJ; Sinsel, NK
      Facial contour restoration in Barraquer-Simons syndrome using two free anterolateral thigh flaps

      PLASTIC AND RECONSTRUCTIVE SURGERY
    42. Gavrilova, O; Marcus-Samuels, B; Graham, D; Kim, JK; Shulman, GI; Castle, AL; Vinson, C; Eckhaus, M; Reitman, ML
      Surgical implantation of adipose tissue reverses diabetes in lipoatrophic mice

      JOURNAL OF CLINICAL INVESTIGATION
    43. Hegele, RA; Cao, HN; Huff, MW; Anderson, CM
      LMNA R482Q mutation in partial lipodystrophy associated with reduced plasma leptin concentration

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    44. Schaffler, A; Barth, N; Palitzsch, KD; Drobnik, W; Scholmerich, J; Schmitz, G
      Mutation analysis of the human adipocyte-specific apM-I gene

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    45. Garg, A
      Lipodystrophies

      AMERICAN JOURNAL OF MEDICINE
    46. Biasi, D; Caramaschi, P; Carletto, A; Bambara, LM
      A case of acquired partial lipodystrophy associated with localized scleroderma and undifferentiated connective tissue disease

      RHEUMATOLOGY INTERNATIONAL
    47. Anderson, JL; Khan, M; David, WS; Mahdavi, Z; Nuttall, FQ; Krech, E; West, SG; Vance, JM; Pericak-Vance, MA; Nance, MA
      Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Chen, DL; Garg, A
      Monogenic disorders of obesity and body fat distribution

      JOURNAL OF LIPID RESEARCH
    49. DEMETRIOU K; KALLIKAS I; ZOUVANI I; KYRIACOU K; PIERIDES A
      THE PREGNANT PATIENT WITH PARTIAL LIPODYSTROPHY DEVELOPING ACUTE-RENAL-FAILURE - ONSET OF DE-NOVO MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS

      Nephrology, dialysis, transplantation
    50. MEYERS KEC; FINN L; KAPLAN BS
      MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS TYPE-III

      Pediatric nephrology
    51. JANSSEN JAMJL; HOOGERBRUGGE N; VANNECK JW; UITTERLINDEN P; LAMBERTS SWJ
      THE IGF-I IGFBP SYSTEM IN CONGENITAL PARTIAL LIPODYSTROPHY/

      Clinical endocrinology
    52. LEVY Y; GEORGE J; YONA E; SHOENFELD Y
      PARTIAL LIPODYSTROPHY, MESANGIOCAPILLARY GLOMERULONEPHRITIS, AND COMPLEMENT DYSREGULATION - AN AUTOIMMUNE PHENOMENON

      Immunologic research
    53. PARDINI VC; VICTORIA IMN; ROCHA SMV; ANDRADE DG; ROCHA AM; PIERONI FB; MILAGRES G; PURISCH S; VELHO G
      LEPTIN LEVELS, BETA-CELL FUNCTION, AND INSULIN SENSITIVITY IN FAMILIES WITH CONGENITAL AND ACQUIRED GENERALIZED LIPOATROPIC DIABETES

      The Journal of clinical endocrinology and metabolism
    54. JACKSON SNJ; PINKNEY J; BARGIOTTA A; VEAL CD; HOWLETT TA; MCNALLY PG; CORRAL R; JOHNSON A; TREMBATH RC
      A DEFECT IN THE REGIONAL DEPOSITION OF ADIPOSE-TISSUE (PARTIAL LIPODYSTROPHY) IS ENCODED BY A GENE AT CHROMOSOME 1Q

      American journal of human genetics
    55. SPRANGER S; SPRANGER M; TASMAN AJ; REITH W; VOIGTLANDER T; VOIGTLANDER V
      BARRAQUER-SIMONS-SYNDROME (WITH SENSORINEURAL DEAFNESS) - A CONTRIBUTION TO THE DIFFERENTIAL-DIAGNOSIS OF LIPODYSTROPHY SYNDROMES

      American journal of medical genetics
    56. URSICH MJM; FUKUI RT; GALVAO MSA; MARCONDES JAM; SANTOMAURO ATMG; SILVA MER; ROCHA DM; WAJCHENBERG BL
      INSULIN-RESISTANCE IN LIMB AND TRUNK PARTIAL LIPODYSTROPHY (TYPE-2 KOBBERLING-DUNNIGAN SYNDROME)

      Metabolism, clinical and experimental
    57. NASR AM; AYYASH I; KARCIOGLU ZA
      UNILATERAL ENOPHTHALMOS SECONDARY TO ACQUIRED HEMILIPODYSTROPHY

      American journal of ophthalmology
    58. WAYTE J; BIRD G; WILKINSON JD
      THE CLINICAL-SIGNIFICANCE OF PARTIAL LIPOATROPHY AND C3 HYPOCOMPLEMENTEMIA - A REPORT OF 2 CASES

      Clinical and experimental dermatology
    59. MEYERS KEC; STRIFE CF; WITZLEBEN C; KAPLAN BS
      DISCORDANT RENAL HISTOPATHOLOGIC FINDINGS AND COMPLEMENT PROFILES IN MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS TYPE-III

      American journal of kidney diseases
    60. WILDERMUTH S; SPRANGER S; SPRANGER M; RAUE F; MEINCK HM
      KOBBERLING-DUNNIGAN SYNDROME - A RARE CAUSE OF GENERALIZED MUSCULAR HYPERTROPHY

      Muscle & nerve
    61. SOTOS JF
      OVERGROWTH

      Clinical pediatrics
    62. STURLEY RH; STIRLING C; RECKLESS JPD
      GENERALIZED LIPODYSTROPHY AND PREGNANCY

      British journal of obstetrics and gynaecology
    63. CARMICHAEL AJ; MARSDEN JR
      URTICARIAL VASCULITIS - A PRESENTATION OF C3 NEPHRITIC FACTOR

      British journal of dermatology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/08/20 alle ore 00:42:01