The Experts below are selected from a list of 273 Experts worldwide ranked by ideXlab platform
Jo-david Fine - One of the best experts on this subject based on the ideXlab platform.
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Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis bullosa: Experience of the National Epidermolysis bullosa Registry, 1986–2002
Journal of Hand Surgery (European Volume), 2020Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
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inherited Epidermolysis bullosa recent basic and clinical advances
Current Opinion in Pediatrics, 2010Co-Authors: Jo-david FineAbstract:Purpose of reviewThis review highlights key findings, both clinical and basic, that have been published in the field of inherited Epidermolysis bullosa within the past few years.Recent findingsNew Epidermolysis bullosa phenotypes, genotypes and modes of transmission have been identified, resulting i
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pseudosyndactyly and musculoskeletal contractures in inherited Epidermolysis bullosa experience of the national Epidermolysis bullosa registry 1986 2002
Journal of Hand Surgery (European Volume), 2005Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
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International Symposium on Epidermolysis bullosa
Journal of Investigative Dermatology, 1994Co-Authors: Jo-david FineAbstract:An international symposium on inherited Epidermolysis bullosa was held at the University of North Carolina at Chapel Hill on April 25–26, 1994. All areas currently of clinical and research interest pertinent to this disease were discussed, ranging from basic epidemiologic issues to the definition of molecular defects in each of the three major types of Epidermolysis bullosa and the potential for gene therapy. A major focus of this meeting was the presentation of data collected by the National Epidermolysis bullosa Registry.
Chirayath M Suchindran - One of the best experts on this subject based on the ideXlab platform.
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Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis bullosa: Experience of the National Epidermolysis bullosa Registry, 1986–2002
Journal of Hand Surgery (European Volume), 2020Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
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pseudosyndactyly and musculoskeletal contractures in inherited Epidermolysis bullosa experience of the national Epidermolysis bullosa registry 1986 2002
Journal of Hand Surgery (European Volume), 2005Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
Joy Deleoz - One of the best experts on this subject based on the ideXlab platform.
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Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis bullosa: Experience of the National Epidermolysis bullosa Registry, 1986–2002
Journal of Hand Surgery (European Volume), 2020Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
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pseudosyndactyly and musculoskeletal contractures in inherited Epidermolysis bullosa experience of the national Epidermolysis bullosa registry 1986 2002
Journal of Hand Surgery (European Volume), 2005Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
David T Devries - One of the best experts on this subject based on the ideXlab platform.
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Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis bullosa: Experience of the National Epidermolysis bullosa Registry, 1986–2002
Journal of Hand Surgery (European Volume), 2020Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
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pseudosyndactyly and musculoskeletal contractures in inherited Epidermolysis bullosa experience of the national Epidermolysis bullosa registry 1986 2002
Journal of Hand Surgery (European Volume), 2005Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
Lorraine Johnson - One of the best experts on this subject based on the ideXlab platform.
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Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis bullosa: Experience of the National Epidermolysis bullosa Registry, 1986–2002
Journal of Hand Surgery (European Volume), 2020Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.
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pseudosyndactyly and musculoskeletal contractures in inherited Epidermolysis bullosa experience of the national Epidermolysis bullosa registry 1986 2002
Journal of Hand Surgery (European Volume), 2005Co-Authors: Jo-david Fine, Lorraine Johnson, Madeline Weiner, Amy Stein, Sydney S Cash, Joy Deleoz, David T Devries, Chirayath M SuchindranAbstract:Mitten deformities of the hands and feet occur in nearly every patient with the most severe subtype (Hallopeau-Siemens) of recessive dystrophic Epidermolysis bullosa, and in at least 40–50% of all other recessive dystrophic Epidermolysis bullosa patients. Smaller numbers of patients with dominant dystrophic, junctional, and simplex types of Epidermolysis bullosa are also at risk of this complication. Surgical intervention is commonly performed to correct these deformities, but recurrence and the need for repeated surgery are common. Higher numbers of Epidermolysis bullosa patients also develop musculoskeletal contractures in other anatomic sites, further impairing overall function. Lifetable analyses not only better project the cumulative risk of mitten deformities and other contractures but also emphasize the need for early surveillance and intervention, since both of these musculoskeletal complications may occur within the first year of life.