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Journal Abstract Search
252 related items for PubMed ID: 19444897
1. The Erlenmeyer flask bone deformity in the skeletal dysplasias. Faden MA, Krakow D, Ezgu F, Rimoin DL, Lachman RS. Am J Med Genet A; 2009 Jun; 149A(6):1334-45. PubMed ID: 19444897 [Abstract] [Full Text] [Related]
2. Sclerosing bone dysplasias--a target-site approach. Greenspan A. Skeletal Radiol; 1991 Jun; 20(8):561-83. PubMed ID: 1776023 [Abstract] [Full Text] [Related]
4. [Differential diagnosis of metaphyseal dysplasias and osteodysplasty (osteodysplasty of Melnick and Needles) (author's transl)]. Böttger E, Kleinsorge H, Wemmer U, Kuhn H, Hebestreit P, Schäfer W. Z Orthop Ihre Grenzgeb; 1978 Jun; 116(6):810-9. PubMed ID: 726565 [Abstract] [Full Text] [Related]
5. Metaphyseal dysplasia: a new autosomal dominant type in a large German kindred. Braun HS, Nürnberg P, Tinschert S. Am J Med Genet; 2001 Jun 01; 101(1):74-7. PubMed ID: 11343343 [Abstract] [Full Text] [Related]
6. Metaphyseal dysplasia of Braun-Tinschert type: report of a Japanese girl. Takata S, Nishimura G, Ikegawa S, Kuroda Y, Nishino M, Matsui Y, Yasui N. Am J Med Genet A; 2006 Jun 01; 140(11):1234-7. PubMed ID: 16691581 [Abstract] [Full Text] [Related]
7. A case with Pyle type metaphyseal dysplasia: clinical, radiological and histological evaluation. Percin EF, Percin S, Koptagel E, Demirel H. Genet Couns; 2003 Jun 01; 14(4):387-93. PubMed ID: 14738111 [Abstract] [Full Text] [Related]
8. Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. I. Familial metaphyseal dysplasia and craniometaphyseal dysplasia; their relation to leontiasis ossea and osteopetrosis; disorders of bone remodeling. JACKSON WP, ALBRIGHT F, DREWRY G, HANELIN J, RUBIN MI. AMA Arch Intern Med; 1954 Dec 01; 94(6):871-85. PubMed ID: 13217486 [No Abstract] [Full Text] [Related]
9. Pyle metaphyseal dysplasia. Gupta N, Kabra M, Das CJ, Gupta AK. Indian Pediatr; 2008 Apr 01; 45(4):323-5. PubMed ID: 18451455 [Abstract] [Full Text] [Related]
16. Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia. Verloes A, Lesenfants S, Barr M, Grange DK, Journel H, Lombet J, Mortier G, Roeder E. Am J Med Genet; 2000 Feb 28; 90(5):407-22. PubMed ID: 10706363 [Abstract] [Full Text] [Related]
17. Pyle metaphyseal dysplasia in an African child: Case report and review of the literature. Wonkam A, Makubalo N, Roberts T, Chetty M. S Afr Med J; 2016 May 25; 106(6 Suppl 1):S110-3. PubMed ID: 27245543 [Abstract] [Full Text] [Related]
18. TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families. Andreucci E, Aftimos S, Alcausin M, Haan E, Hunter W, Kannu P, Kerr B, McGillivray G, McKinlay Gardner RJ, Patricelli MG, Sillence D, Thompson E, Zacharin M, Zankl A, Lamandé SR, Savarirayan R. Orphanet J Rare Dis; 2011 Jun 09; 6():37. PubMed ID: 21658220 [Abstract] [Full Text] [Related]
19. Sclerosing bone dysplasias: genetic and radioclinical features. Vanhoenacker FM, De Beuckeleer LH, Van Hul W, Balemans W, Tan GJ, Hill SC, De Schepper AM. Eur Radiol; 2000 Jun 09; 10(9):1423-33. PubMed ID: 10997431 [Abstract] [Full Text] [Related]