These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

64 related articles for article (PubMed ID: 9541481)

  • 1. "A rare disorder, yes; an unimportant one, never".
    Olsen BR
    J Clin Invest; 1998 Apr; 101(8):1545-6. PubMed ID: 9541481
    [No Abstract]   [Full Text] [Related]  

  • 2. Increased proliferation of osteoblastic cells expressing the activating Gs alpha mutation in monostotic and polyostotic fibrous dysplasia.
    Marie PJ; de Pollak C; Chanson P; Lomri A
    Am J Pathol; 1997 Mar; 150(3):1059-69. PubMed ID: 9060842
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cellular and molecular basis of fibrous dysplasia.
    Marie PJ
    Histol Histopathol; 2001 Jul; 16(3):981-8. PubMed ID: 11510989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Etiology of fibrous dysplasia and McCune-Albright syndrome.
    Cohen MM; Howell RE
    Int J Oral Maxillofac Surg; 1999 Oct; 28(5):366-71. PubMed ID: 10535539
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pseudohypoparathyroidism: history of the disease.
    de Sanctis L
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():627-33. PubMed ID: 16789627
    [No Abstract]   [Full Text] [Related]  

  • 6. [Albright hereditary osteodystrophy].
    Tohma T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):131-2. PubMed ID: 11057167
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. 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]  

  • 9. [McCune-Albright syndrome].
    Yamada N; Tatsuno I
    Nihon Rinsho; 2006 Jun; Suppl 2():126-30. PubMed ID: 16817366
    [No Abstract]   [Full Text] [Related]  

  • 10. McCune-Albright syndrome: radiological and MR findings.
    Yongjing G; Huawei L; Zilai P; Bei D; Hao J; Kemin C
    JBR-BTR; 2001; 84(6):250-2. PubMed ID: 11817476
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Different genotype of periosteal and endosteal cells of a patient with polyostotic fibrous dysplasia.
    Kitoh H; Yamada Y; Nogami H
    J Med Genet; 1999 Sep; 36(9):724-5. PubMed ID: 10507737
    [No Abstract]   [Full Text] [Related]  

  • 12. Gs alpha-related precocious puberty in females: focus on treatment.
    Hannon TS
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():605-6. PubMed ID: 16789623
    [No Abstract]   [Full Text] [Related]  

  • 13. Tocilizumab in the treatment of a polyostotic variant of fibrous dysplasia of bone.
    de Boysson H; Johnson A; Hablani N; Hajlaoui W; Auzary C; Geffray L
    Rheumatology (Oxford); 2015 Sep; 54(9):1747-9. PubMed ID: 26070936
    [No Abstract]   [Full Text] [Related]  

  • 14. Searching for Arg201 mutations in the GNAS1 gene in Italian patients with McCune-Albright syndrome.
    de Sanctis L; Romagnolo D; Greggio N; Genitori L; Lala R; de Sanctis C
    J Pediatr Endocrinol Metab; 2002; 15 Suppl 3():883-9. PubMed ID: 12199346
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rare bone disorders reveal a key metabolic gene.
    Senior K
    Trends Mol Med; 2001 Feb; 7(2):45-6. PubMed ID: 11286735
    [No Abstract]   [Full Text] [Related]  

  • 16. Activating Gs a mutation rarely occurs in musculoskeletal tumors other than fibrous dysplasia.
    Gu W; Ogose A; Matsuba A; Kawashima H; Hotta T; Kudo N; Hoshino M; Kondo N; Mera H; Endo N
    Anticancer Res; 2006; 26(2B):1611-4. PubMed ID: 16619580
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of the GSalpha gene in the diagnosis of fibrous dysplasia.
    Perdigão PF; Pimenta FJ; Castro WH; De Marco L; Gomez RS
    Int J Oral Maxillofac Surg; 2004 Jul; 33(5):498-501. PubMed ID: 15183415
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Is McCune-Albright syndrome overlooked in subjects with fibrous dysplasia of bone?
    Hannon TS; Noonan K; Steinmetz R; Eugster EA; Levine MA; Pescovitz OH
    J Pediatr; 2003 May; 142(5):532-8. PubMed ID: 12756386
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Activating and inactivating mutations in the human GNAS1 gene.
    Aldred MA; Trembath RC
    Hum Mutat; 2000 Sep; 16(3):183-9. PubMed ID: 10980525
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Subcutaneous calcifications and dysmorphic syndrome].
    Avenel G; Bernet J; Lahaxe L; Lévesque H; Marie I
    Rev Med Interne; 2010 Mar; 31(3):238-40. PubMed ID: 19329231
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.