The Experts below are selected from a list of 1617 Experts worldwide ranked by ideXlab platform

Giulia Maria Stella - One of the best experts on this subject based on the ideXlab platform.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary respiratory medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary Respiratory Medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Background: Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. Case presentation: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. Conclusion: This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

Rosaria Cortese - One of the best experts on this subject based on the ideXlab platform.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary respiratory medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary Respiratory Medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Background: Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. Case presentation: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. Conclusion: This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

Salvatore Savasta - One of the best experts on this subject based on the ideXlab platform.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary respiratory medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary Respiratory Medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Background: Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. Case presentation: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. Conclusion: This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

Silvia Di Stasi - One of the best experts on this subject based on the ideXlab platform.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary respiratory medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary Respiratory Medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Background: Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. Case presentation: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. Conclusion: This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

Tiziana Boggini - One of the best experts on this subject based on the ideXlab platform.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary respiratory medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.

  • Lung disease recalling paraseptal emphysema in a patient with Goltz Syndrome
    Multidisciplinary Respiratory Medicine, 2016
    Co-Authors: Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella
    Abstract:

    Background: Goltz Syndrome is a rare, genetic disorder mainly occurring in female patients. Case presentation: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz Syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz Syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions. Conclusion: This report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz Syndrome at least in its autosomal form.