ACNP - Italian Periodicals Catalogue

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Results: 1-10 |

Results: 10

Fibrodysplasia ossificans progressiva

Authors: Mahboubi, S Glaser, DL Shore, EM Kaplan, FS

Citation: S. Mahboubi et al., Fibrodysplasia ossificans progressiva, PEDIAT RAD, 31(5), 2001, pp. 307-314

Mast cell involvement in fibrodysplasia ossificans progressiva

Authors: Gannon, FH Glaser, D Caron, R Thompson, LDR Shore, EM Kaplan, FS

Citation: Fh. Gannon et al., Mast cell involvement in fibrodysplasia ossificans progressiva, HUMAN PATH, 32(8), 2001, pp. 842-848

GNAS1 mutation and Cbfa1 misexpression in a child with severe congenital platelike osteoma cutis

Authors: Yeh, GL Mathur, S Wivel, A Li, M Gannon, FH Ulied, A Audi, L Olmsted, EA Kaplan, FS Shore, EM

Citation: Gl. Yeh et al., GNAS1 mutation and Cbfa1 misexpression in a child with severe congenital platelike osteoma cutis, J BONE MIN, 15(11), 2000, pp. 2063-2073

Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification

Authors: Eddy, MC De Beur, SMJ Yandow, SM McAlister, WH Shore, EM Kaplan, FS Whyte, MP Levine, MA

Citation: Mc. Eddy et al., Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification, J BONE MIN, 15(11), 2000, pp. 2074-2083

Progressive osseous heteroplasia

Authors: Kaplan, FS Shore, EM

Citation: Fs. Kaplan et Em. Shore, Progressive osseous heteroplasia, J BONE MIN, 15(11), 2000, pp. 2084-2094

Osteogenic induction in hereditary disorders of heterotopic ossification

Authors: Shore, EM Glaser, DL Gannon, FH

Citation: Em. Shore et al., Osteogenic induction in hereditary disorders of heterotopic ossification, CLIN ORTHOP, (374), 2000, pp. 303-316

Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)

Authors: Xu, MQ Feldman, G Le Merrer, M Shugart, YY Glaser, DL Urtizberea, JA Fardeau, M Connor, JM Triffitt, J Smith, R Shore, EM Kaplan, FS

Citation: Mq. Xu et al., Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP), CLIN GENET, 58(4), 2000, pp. 291-298

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31

Authors: Feldman, G Li, M Martin, S Urbanek, M Urtizberea, JA Fardeau, M LeMerrer, M Connor, JM Triffitt, J Smith, R Muenke, M Kaplan, FS Shore, EM

Citation: G. Feldman et al., Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31, AM J HU GEN, 66(1), 2000, pp. 128-135

Fibrodysplasia ossificans progressiva

Authors: Shore, EM Rogers, JG Smith, R Gannon, FH Delatycki, M Urtizberea, JA Triffitt, J Le Merrer, M Kaplan, FS

Citation: Em. Shore et al., Fibrodysplasia ossificans progressiva, GENETICS OF OSTEOPOROSIS AND METABOLIC BONE DISEASE, 2000, pp. 211-236

Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva

Authors: Virdi, AS Shore, EM Oreffo, ROC Li, M Connor, JM Smith, R Kaplan, FS Triffitt, JT

Citation: As. Virdi et al., Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva, CALCIF TIS, 65(3), 1999, pp. 250-255

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