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 *

113 related articles for article (PubMed ID: 8152878)

  • 1. Sponastrime dysplasia: report on two siblings with metal retardation.
    Camera G; Camera A; Di Rocco M; Gatti R
    Pediatr Radiol; 1993; 23(8):611-4. PubMed ID: 8152878
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sponastrime dysplasia: report on a male patient.
    Camera G; Camera A; Pozzolo S; Costa P
    Pediatr Radiol; 1994; 24(5):322-4. PubMed ID: 7824362
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterogeneity of SPONASTRIME dysplasia: delineation of a variant form with severe mental retardation.
    Verloes A; Misson JP; Dubru JM; Jamblin P; Le Merrer M
    Clin Dysmorphol; 1995 Jul; 4(3):208-15. PubMed ID: 7551156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Relationships between skeletal development and mental disorders].
    Silinkovà-Màlkovà E; Balcar V; Silink K; Kremenovà J; Blehovà B
    Cesk Radiol; 1973; 27(4):217-27. PubMed ID: 4726588
    [No Abstract]   [Full Text] [Related]  

  • 5. Sjögren-Larsson syndrome with epiphyseal-metaphyseal dysplasia.
    Ozonoff MB; Ogden JA
    Am J Roentgenol Radium Ther Nucl Med; 1973 May; 118(1):187-92. PubMed ID: 4634106
    [No Abstract]   [Full Text] [Related]  

  • 6. SPONASTRIME dysplasia: report of an 11-year-old boy and review of the literature.
    Cooper HA; Crowe J; Butler MG
    Am J Med Genet; 2000 May; 92(1):33-9. PubMed ID: 10797420
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Lenz-Majewski hyperostotic dwarfism. A syndrome of multiple congenital anomalies, mental retardation, and progressive skeletal sclerosis.
    Robinow M; Johanson AJ; Smith TH
    J Pediatr; 1977 Sep; 91(3):417-21. PubMed ID: 894410
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The SPONASTRIME dysplasia: familial short-limb dwarfism with saddle nose, spinal alterations and metaphyseal striation. Report of 4 siblings.
    Fanconi S; Issler C; Giedion A; Prader A
    Helv Paediatr Acta; 1983 Aug; 38(3):267-80. PubMed ID: 6618893
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sponastrime dysplasia. A radiologic-pathologic correlation.
    Lachman RS; Stoss H; Spranger J
    Pediatr Radiol; 1989; 19(6-7):417-24. PubMed ID: 2771481
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sponastrime dysplasia: diagnostic criteria based on five new and six previously published cases.
    Langer LO; Beals RK; Scott CI
    Pediatr Radiol; 1997 May; 27(5):409-14. PubMed ID: 9133352
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SPONASTRIME dysplasia: report on a female patient with severe skeletal changes.
    Masuno M; Nishimura G; Adachi M; Hotsubo T; Tachibana K; Makita Y; Imaizumi K; Kuroki Y
    Am J Med Genet; 1996 Dec; 66(4):429-32. PubMed ID: 8989461
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Asphyxiating thoracic dysplasia as a complication of metaphyseal chondrodysplasia (Jansen type).
    Ozonoff MB
    Birth Defects Orig Artic Ser; 1974; 10(12):72-7. PubMed ID: 4461094
    [No Abstract]   [Full Text] [Related]  

  • 13. [Idiopathic multicentric osteolysis with craniodysplasis and mental retardation: a new syndrome? (author's transl)].
    Mathias K; Ludwig U
    Rofo; 1977 Sep; 127(3):255-61. PubMed ID: 143430
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Report of a case: acromesomelic dysplasia: radiologic, clinical, and pathological study.
    Fernández del Moral R; Santolaya Jiménez JM; Rodríguez González JI; Franco Vicario R
    Am J Med Genet; 1989 Jul; 33(3):415-9. PubMed ID: 2801778
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ruvalcaba syndrome: a case report.
    Bianchi E; Livieri C; Arico M; Cattaneo E; Podesta AF; Beluffi G
    Eur J Pediatr; 1984 Sep; 142(4):301-3. PubMed ID: 6489381
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Another observation of Langer-type sponastrime dysplasia variant.
    Nishimura G; Mikawa M; Fukushima Y
    Am J Med Genet; 1998 Nov; 80(3):288-90. PubMed ID: 9843056
    [No Abstract]   [Full Text] [Related]  

  • 17. Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation.
    Geneviève D; Héron D; El Ghouzzi V; Prost-Squarcioni C; Le Merrer M; Jacquette A; Sanlaville D; Pinton F; Villeneuve N; Kalifa G; Munnich A; Cormier-Daire V
    Eur J Hum Genet; 2005 May; 13(5):541-6. PubMed ID: 15726110
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pseudodiastrophic dysplasia: a distinct newborn skeletal dysplasia.
    Eteson DJ; Beluffi G; Burgio GR; Belloni C; Lachman RS; Rimoin DL
    J Pediatr; 1986 Oct; 109(4):635-41. PubMed ID: 3761077
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.
    Gurrieri F; Sammito V; Bellussi A; Neri G
    Am J Med Genet; 1992 Oct; 44(3):315-20. PubMed ID: 1488978
    [No Abstract]   [Full Text] [Related]  

  • 20. A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus.
    Lowry B; Miller JR; Fraser FC
    Am J Dis Child; 1971 Jun; 121(6):496-500. PubMed ID: 5581017
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.