Francomano, Clair A.
Clair A. Francomano
VIAF ID: 69020192 (Personal)
Permalink: http://viaf.org/viaf/69020192
Preferred Forms
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100 0 _ ‡a Clair A. Francomano
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200 _ | ‡a Francomano ‡b Clair A.
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100 1 _ ‡a Francomano, Clair A
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100 1 _ ‡a Francomano, Clair A.
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100 1 _ ‡a Francomano, Clair A. (sparse)
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100 1 0 ‡a Francomano, Clair A.
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100 1 _ ‡a Francomano, Clair A.
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4xx's: Alternate Name Forms (4)
Works
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Association of Chiari malformation type I and tethered cord syndrome: preliminary results of sectioning filum terminale |
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Atlanto-axial rotary instability (Fielding type 1): characteristic clinical and radiological findings, and treatment outcomes following alignment, fusion, and stabilization |
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Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome. |
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Case 47: dural ectasia associated with Marfan syndrome |
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A central nervous system specific mouse model for thanatophoric dysplasia type II. |
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Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF-β expression and connective tissue features |
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Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case report |
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Complementary medicine and genetic medicine: polar disciplines or dynamic partners? |
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Consensus clinical management guidelines for Alström syndrome |
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Defining renal phenotype in Alström syndrome |
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Echocardiographic findings in classical and hypermobile Ehlers-Danlos syndromes |
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Gene expression profile of human bone marrow stromal cells: high-throughput expressed sequence tag sequencing analysis |
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Genetics in clinical practice. |
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Growth and integration of neocartilage with native cartilage in vitro. |
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Heritable disorders of connective tissue: Description of a data repository and initial cohort characterization |
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Hyaline cartilage engineered by chondrocytes in pellet culture: histological, immunohistochemical and ultrastructural analysis in comparison with cartilage explants. |
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Iden kango no jissen : Jirei karano apurōchi |
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The influence of pulsed low-intensity ultrasound on matrix production of chondrocytes at different stages of differentiation: an explant study |
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The international consortium on the Ehlers-Danlos syndromes. |
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Issues surrounding prenatal genetic testing for achondroplasia |
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Klotho gene variation and expression in 20 inbred mouse strains. |
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Letter to the editor regarding "Atlantoaxial dislocation due to os odontoideum in patients with Down's syndrome: literature review and case reports" |
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Living with achondroplasia: quality of life evaluation following cervico-medullary decompression |
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The major mutation in the RMRP gene causing CHH among the Amish is the same as that found in most Finnish cases. |
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Medical genetic studies in the Amish: historical perspective |
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Mendelian inheritance in man, 1990: |
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The mutational spectrum of brachydactyly type C |
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n89100075 |
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Pain and sleep quality in children with non-vascular Ehlers-Danlos syndromes |
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Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndrome |
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Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model |
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Resistance to local anesthesia in people with the Ehlers-Danlos Syndromes presenting for dental surgery |
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Small deletions in the type II collagen triple helix produce Kniest dysplasia |
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Stickler syndrome: clinical characteristics and diagnostic criteria |
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The Stickler syndrome: genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1. |
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Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia |
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Survey of Ehlers-Danlos Patients' ophthalmic surgery experiences |
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Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and Chiari malformation Type I in patients with hereditary disorders of connective tissue |
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Use of Cluster Analysis to Delineate Symptom Profiles in an Ehlers-Danlos Syndrome Patient Population |
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Use of prescription opioid and other drugs among a cohort of persons with Ehlers-Danlos syndrome: A retrospective study |
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Victor McKusick and the history of medical genetics |
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遺伝看護の実践 : 事例からのアプローチ |
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