BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 18799944)

  • 1. Pseudohypoparathyroidism Ia with Evans syndrome.
    Pavone P; Praticò AD; Castellano-Chiodo D; Ruggieri M
    J Pediatr Hematol Oncol; 2008 Aug; 30(8):628-30. PubMed ID: 18799944
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Presentation and clinical progression of pseudohypoparathyroidism with multi-hormone resistance and Albright hereditary osteodystrophy: a case series.
    Gelfand IM; Eugster EA; DiMeglio LA
    J Pediatr; 2006 Dec; 149(6):877-880. PubMed ID: 17137912
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early manifestation of obesity and calcinosis cutis in infantile pseudohypoparathyroidism.
    Poomthavorn P; Zacharin M
    J Paediatr Child Health; 2006 Dec; 42(12):821-3. PubMed ID: 17096721
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation].
    Derrien C; Odent S; Henry C; De La Villemarque R; Poirier JY; Maugendre D
    Ann Endocrinol (Paris); 2001 Dec; 62(6):529-33. PubMed ID: 11845029
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Evans syndrome associated with idiopathic mixed-type autoimmune hemolytic anemia].
    Kakinoki Y; Nagase M; Okada K; Chiba K; Fukuhara T; Miyake T
    Rinsho Ketsueki; 2008 Jul; 49(7):516-20. PubMed ID: 18709985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pubertal development in patients with McCune-Albright syndrome or pseudohypoparathyroidism.
    de Sanctis C; Lala R; Matarazzo P; Andreo M; de Sanctis L
    J Pediatr Endocrinol Metab; 2003 Mar; 16 Suppl 2():293-6. PubMed ID: 12729407
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Albright's hereditary osteodystrophy: report of three cases].
    Bujan MM; Cervini AB; Fano V; Pierini AM
    Arch Argent Pediatr; 2010 Apr; 108(2):e24-7. PubMed ID: 20467695
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Albright hereditary osteodystrophy: identification of a novel mutation in a family].
    Bastida Eizaguirre M; Iturbe Ortiz De Urbina R; Arto Urzainqui M; Ezquerra Larreina R; Escalada San Martín J
    An Esp Pediatr; 2001 Jun; 54(6):598-600. PubMed ID: 11412411
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Immunologic thrombopenic purpura associated with an autoimmune hemolytic anemia or Fisher-Evans syndrome: apropos of a case].
    Ndiaye O; Sylla A; Ndiaye FS; Diagne I; Diallo-Chauvin M; Diouf S; Sallm G; Kuakuvi K
    Dakar Med; 1999; 44(2):240-2. PubMed ID: 11957294
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Basedow disease associated with Evans syndrome].
    Kuroda H; Kida M; Watanabe H; Matsunaga T; Niitsu Y; Matsumoto M
    Rinsho Ketsueki; 2005 Oct; 46(10):1118-22. PubMed ID: 16440774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Type I pseudohypoparathyroidism. Study and prolonged follow-up of a case].
    Pardos LC; Buñuel C; Antón R; García C; Lasarte JJ; Mayayo E; Ferrández A
    An Esp Pediatr; 1989 Sep; 31(3):240-7. PubMed ID: 2631607
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A rare condition associated with celiac disease: Evans syndrome.
    Yarali N; Demirceken F; Kondolat M; Ozkasap S; Kara A; Tunc B
    J Pediatr Hematol Oncol; 2007 Sep; 29(9):633-5. PubMed ID: 17805039
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Visceral leishmaniasis presented with Evans syndrome: a case report.
    Alioglu B; Avci Z; Ozyurek E; Ozbek N
    Am J Hematol; 2007 Nov; 82(11):1030-1. PubMed ID: 17626253
    [No Abstract]   [Full Text] [Related]  

  • 14. [Late onset epilepsy as the first symptom of pseudohypoparathyroidism].
    Villarreal-Núñez F; Adames-Quintero AE; Noriega L
    Rev Neurol; 2005 Aug 1-15; 41(3):155-8. PubMed ID: 16047299
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case of pseudohypoparathyroidism].
    Bednarek-Tupikowska G
    Przegl Lek; 1999; 56(11):743-6. PubMed ID: 10800589
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linear skin atrophy preceding calcinosis cutis in pseudo-pseudohypoparathyroidism.
    Lau K; Willig RP; Hiort O; Hoeger PH
    Clin Exp Dermatol; 2012 Aug; 37(6):646-8. PubMed ID: 22299648
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
    Nakamoto JM; Sandstrom AT; Brickman AS; Christenson RA; Van Dop C
    Am J Med Genet; 1998 May; 77(4):261-7. PubMed ID: 9600732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Parathyroid insufficiency syndrome. Two new cases: type Ia pseudohypoparathyroidism and pseudo-idiopathic hypoparathyroidism].
    Barajas de Frutos D; Pedrero Vera J; Bolívar Barrales JE; Espigares Martín R; Ortega Martos L; Vílchez Joya R; Bolívar Galiano V; Morell Bernabé JJ
    An Esp Pediatr; 1989 Oct; 31(4):385-8. PubMed ID: 2560613
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oral manifestations of Albright hereditary osteodystrophy: a case report.
    Gomes MF; Camargo AM; Sampaio TA; Graziozi MA; Armond MC
    Rev Hosp Clin Fac Med Sao Paulo; 2002; 57(4):161-6. PubMed ID: 12244336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Cutaneous osteoma and Albright's hereditary osteodystrophy].
    Canillot S; Chouvet B; Besançon C; Perrot H
    Ann Dermatol Venereol; 1994; 121(5):408-13. PubMed ID: 7702269
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.