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Książki na temat „Epidermolysis bullosa”

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Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 9 marca 2023

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Sprawdź 37 najlepszych książek naukowych na temat „Epidermolysis bullosa”.

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1

Lin, Andrew N., i D. Martin Carter, red. Epidermolysis Bullosa. New York, NY: Springer New York, 1992. http://dx.doi.org/10.1007/978-1-4612-2914-8.

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2

Fine, Jo-David, i Helmut Hintner, red. Life with Epidermolysis Bullosa (EB). Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-79271-1.

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Weiß, Hedwig, i Florian Prinz. Occupational Therapy in Epidermolysis Bullosa. Vienna: Springer Vienna, 2013. http://dx.doi.org/10.1007/978-3-7091-1139-0.

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N, Lin Andrew, i Carter D. Martin 1936-, red. Epidermolysis bullosa: Basic and clinical aspects. New York: Springer-Verlag, 1992.

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5

Jo-David, Fine, i National Epidermolysis Bullosa Registry (U.S.), red. Epidermolysis bullosa: Clinical, epidemiologic, and laboratory advances, and the findings of the National Epidermolysis Bullosa Registry. Baltimore: Johns Hopkins University Press, 1999.

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6

Parker, James N., i Philip M. Parker. The official patient's sourcebook on epidermolysis bullosa. Redaktorzy Icon Group International Inc i NetLibrary Inc. San Diego, Calif: Icon Health Publications, 2002.

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7

Kennedy, Jonny. Jonny Kennedy: The story of the boy whose skin fell off. Newcastle upon Tyne: Tonto, 2007.

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8

Florian, Prinz, red. Occupational therapy in epidermolysis bullosa: A holistic concept for intervention from infancy to adult. Wien: Springer, 2013.

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9

Helmut, Hintner, i SpringerLink (Online service), red. Life with Epidermolysis Bullosa (EB): Etiology, Diagnosis, Multidisciplinary Care and Therapy. Vienna: Springer Vienna, 2009.

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10

C, Priestley G., red. Epidermolysis bullosa: A comprehensive review of classification, management and laboratory studies. Crowthorne: Dystrophic Epidermolysis Bullosa Research Association, 1990.

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11

Nicola, Cirillo. Techniques in epidermal biology: An integrated approach to autoimmune skin disease. Hauppauge, N.Y: Nova Science Publishers, 2011.

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12

Paediatric skin and wound care. Aberdeen: Wounds UK, 2006.

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13

Samol, Nancy B., i Eric P. Wittkugel. Epidermolysis Bullosa. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0065.

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Epidermolysis bullosa (EB) is a genetic skin disorder with multiple modes of inheritance that causes blister formation from shear injury and results in extensive scarring. Children with EB provide an array of unique challenges when presenting for anesthetic care. Anticipation and management of a potentially difficult airway as well as the protection of fragile skin and mucous membranes are high priorities during anesthetic planning. Complications can arise with use of even the most routine anesthesia monitors and placement of a simple peripheral IV line. Thorough preoperative planning and meticulous perioperative care will reduce complications and result in a smooth anesthetic for both patient and clinician.

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14

Nguyen, Kim-Phuong. Epidermolysis Bullosa. Redaktorzy Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel i Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0060.

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The anesthetic management of children with epidermolysis bullosa (EB) presents unique challenges to the pediatric anesthesiologist. Preoperative planning includes anticipation of a potentially difficult airway, focused protection of fragile skin and mucous membranes, and special consideration in the placement of standard monitors and intravenous access. Additionally, this chapter highlights the natural history and common procedures that may be performed in a child with EB; this will help prepare the anesthesiologist and the patient for a smooth anesthetic course. This chapter presents the case study of a 10-year-old girl with a medical history of recessive dystrophic EB, esophageal strictures, and poor nutritional status, who presents for esophageal dilation and percutaneous endoscopic gastrostomy tube placement.

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15

Sybert, Virginia P. Disorders of The Epidermis: Differentiation and Kinetics. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0002.

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Ichthyoses – Bullous Congenital Ichthyosiform Erythroderma – Continual Peeling Skin – Harlequin Fetus – Ichthyosis Bullosa of Siemens – Ichthyosis Hystrix – Ichthyosis Vulgaris – Lamellar Exfoliation of the Newborn – Lamellar Ichthyosis/Nonbullous Congenital Ichthyosiform Erythroderma – Netherton Syndrome – Restrictive Dermopathy – X-linked Recessive Ichthyosis – Erythrokeratodermas – Erythrokeratodermia Variabilis – Pityriasis Rubra Pilaris – Progressive Symmetric Erythrokeratoderma – Acrokeratoderma – Acrokeratoelastoidosis – Acrokeratosis Verruciformis (HOPF) – Hereditary Palmoplantar Keratodermas – Hereditary Palmoplantar Keratoderma with Deafness – Hereditary Palmoplantar Keratoderma Epidermolytic Hyperkeratosis – Hereditary Palmoplantar Keratoderma Howel-Evans – Hereditary Palmoplantar Keratoderma Olmsted – Hereditary Palmoplantar Keratoderma Punctate – Hereditary Palmoplantar Keratoderma Striata – Hereditary Palmoplantar Keratoderma Unna-Thost – Hereditary Palmoplantar Keratoderma Vohwinkel – Keratolytic Winter Erythema – Mal de Meleda – Papillon-Lefèvre – Scleroatrophic and Keratotic Dermatosis of the Limbs – Porokeratoses – Porokeratosis of Mibelli – Other Disorders of the Epidermis – Absence of Dermatoglyphics – Acanthosis Nigricans – Darier-White Disease – Hereditary Painful Callosities – Keratosis Follicularis Spinulosa Decalvans – Knuckle Pads – Kyrle/Flegel Disease – Ulerythema Ophryogenes – Syndromic Disorders – CHILD Syndrome – Chondrodysplasia Punctata – Ichthyosis with Hypogonadism – KID Syndrome – Neu-Laxova Syndrome – Neutral Lipid Storage Disease with Ichthyosis – Refsum Disease – Richner-Hanhart Syndrome – Sjögren-Larsson Syndrome – Cohesion – Epidermolysis Bullosa – Epidermolysis Bullosa Simplex Dowling-Meara – Epidermolysis Bullosa Simplex Generalized – Epidermolysis Bullosa Simplex Localized – Epidermolysis Bullosa Junctional Generalized – Epidermolysis Bullosa Junctional Generalized Atrophic Benign – Epidermolysis Bullosa Dystrophica Cockayne-Touraine – Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens – Epidermolysis Bullosa Dystrophica Pretibial – Transient Bullous Dermolysis of the Newborn – Hailey-Hailey Disease

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16

Jo-David, Fine Helmut Hintner. Life with Epidermolysis Bullosa. Springer, 2009.

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17

C, Silvia. Living with Epidermolysis Bullosa. Lulu.com, 2007.

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18

Sybert, Virginia P. Disorders of the Epidermis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0002.

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Chapter 2 covers Ichthyoses (Bullous Congenital Ichthyosiform Erythroderma, Harlequin Ichthyosis, Ichthyosis Bullosa of Siemens, Ichthyosis Hystrix, Ichthyosis Vulgaris, Lamellar Exfoliation of the Newborn, Lamellar Ichthyosis/Nonbullous Congenital Ichthyosiform Erythroderma, Netherton Syndrome, Peeling Skin Syndrome, Restrictive Dermopathy, and X-linked Recessive Ichthyosis), Erythrokeratodermas (Erythrokeratodermia Variabilis ET PROGESSIVA, and Pityriasis Rubra Pilaris), Acrokeratoderma (Acrokeratoelastoidosis, Acrokeratosis Verruciformis (HOPF)), Hereditary Palmoplantar Keratodermas (Hereditary Palmoplantar Keratoderma with Deafness, Hereditary Palmoplantar Keratoderma Epidermolytic Hyperkeratosis, Hereditary Palmoplantar Keratoderma Howel-Evans, Hereditary Palmoplantar Keratoderma Olmsted, Hereditary Palmoplantar Keratoderma Punctate, Hereditary Palmoplantar Keratoderma Striata, Hereditary Palmoplantar Keratoderma Unna-Thost, Hereditary Palmoplantar Keratoderma Vohwinkel, Keratolytic Winter Erythema, Mal de Meleda, Papillon-Lefèvre, Scleroatrophic and Keratotic Dermatosis of the Limbs), Porokeratoses (Porokeratosis of Mibelli), Other Disorders of the Epidermis (Absence of Dermatoglyphics, Acanthosis Nigricans, Darier-White Disease, Hereditary Painful Callosities, Keratosis Follicularis Spinulosa Decalvans, Knuckle Pads, Kyrle/Flegel Disease, Ulerythema Ophryogenes), Syndromic Disorders (CHILD Syndrome, Chondrodysplasia Punctata, Ichthyosis with Hypogonadism, KID Syndrome, Neu-Laxova Syndrome, Neutral Lipid Storage Disease with Ichthyosis, Refsum Disease, Richner-Hanhart Syndrome, Sjögren-Larsson Syndrome), Cohesion (Epidermolysis Bullosa, Epidermolysis Bullosa Simplex Dowling-Meara, Epidermolysis Bullosa Simplex Generalized, Epidermolysis Bullosa Simplex Localized, Epidermolysis Bullosa Junctional Generalized, Epidermolysis Bullosa Junctional Generalized Atrophic Benign, Epidermolysis Bullosa Dystrophica Cockayne-Touraine, Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens, Epidermolysis Bullosa Dystrophica Pretibial, Transient Bullous Dermolysis of the Newborn, Hailey-Hailey Disease). Each condition is discussed in detail, including dermatologic features, associated anomalies, histopathology, basic defect, treatment, mode of inheritance, prenatal diagnosis, and differential diagnosis.

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19

Lin, Andrew N. Epidermolysis Bullosa: Basic and Clinical Aspects. Springer, 2011.

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20

Lin, Andrew N., i D. Martin Carter. Epidermolysis Bullosa: Basic and Clinical Aspects. Springer London, Limited, 2012.

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21

Epidermolysis Bullosa: Basic and Clinical Aspects. Springer, 2011.

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22

(Editor), Andrew N. Lin, i D. Martin Carter (Editor), red. Epidermolysis Bullosa: Basic and Clinical Aspects. Springer, 1992.

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23

Epidermolysis Bullosa: Pathogenesis and Clinical Features. Elsevier - Health Sciences Division, 2010.

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24

(Editor), Jo-David Fine, Eugene A. Bauer (Editor), Joseph McGuire (Editor) i Alan Moshell (Editor), red. Epidermolysis Bullosa: Clinical, Epidemiologic, and Laboratory Advances and the Findings of the National Epidermolysis Bullosa Registry. The Johns Hopkins University Press, 1999.

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25

Mullins, Hubert. Epidermolysis Bullosa: Prevalence, Clinical Manifestations and Management. Nova Science Publishers, Incorporated, 2016.

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26

Burgart, Alyssa M., i Louise K. Furukawa. Perioperative Care of Patients with Epidermolysis Bullosa. Redaktorzy Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi i Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0065.

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Inherited epidermolysis bullosa comprises a group of rare, serious conditions affecting multiple organ systems. While generally referred to as a dermatologic condition, any organ with an epithelial surface is affected, leading to serious extracutaneous manifestations. These have wide-ranging implications for anesthetic management, including airway management, vascular access, skin protection, and effective pain control. A successful and safe patient experience requires thoughtful evaluation, communication with a multidisciplinary team, anesthetic planning, intraoperative management, and postoperative care. The scenario in this chapter takes readers through a series of questions to enhance their understanding of the disease and how to address common anesthetic problems. Particular attention is paid to suggested monitor modification.

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27

Epidermolysis Bullosa - Diagnosis and Management Pt. II: Dermatologic Clinics. Elsevier - Health Sciences Division, 2010.

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28

Bauer, Johann, Jo-David Fine, Helmut Hintner, Christopher Lanschützer, Martin Laimer, Gabriela Pohla-Gubo, Elke Nischler, Robin A. Eady i Alfred Klausegger. Life with Epidermolysis Bullosa: Etiology, Diagnosis, Multidisciplinary Care and Therapy. Springer, 2011.

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29

Lichen ruber. Pityriasis rubra pilaris. Epidermolysis bullosa. Impetigo herpetiformis. Pemphigus. Springer, 2031.

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30

Tough cookie. New Leaf Press, 1991.

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31

Publications, ICON Health. Epidermolysis Bullosa - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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32

Davies, Emily. Bullous disorders. Redaktorzy Patrick Davey i David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0252.

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This chapter focuses on immunobullous diseases. The immunobullous disorders are a group of diseases in which pathogenic autoantibodies bind to target antigens either in desmosomes (intra-epidermal intracellular adhesion junctions) or in part of the basement membrane zone, resulting in loss of adhesion, and blister formation. This chapter will focus on pemphigus vulgaris, pemphigus foliaceus, bullous pemphigoid, linear IgA disease, chronic bullous disease of childhood, and dermatitis herpetiformis; it will also mention mucous membrane pemphigoid, pemphigoid gestationis, and epidermolysis bullosa acquisita.

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33

Weiß, Hedwig, i Florian Prinz. Occupational Therapy in Epidermolysis bullosa: A holistic Concept for Intervention from Infancy to Adult. Springer, 2016.

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34

Weiß, Hedwig, i Florian Prinz. Occupational Therapy in Epidermolysis bullosa: A holistic Concept for Intervention from Infancy to Adult. Springer, 2012.

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35

Weiß, Hedwig, i Florian Prinz. Occupational Therapy in Epidermolysis Bullosa: A Holistic Concept for Intervention from Infancy to Adult. Springer London, Limited, 2012.

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Hain, Richard D. W., i Satbir Singh Jassal. Skin symptoms. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198745457.003.0014.

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Skin symptoms are commonly seen in paediatric palliative medicine. This chapter covers important skin symptoms, including epidermolysis bullosa, pruritus, fungating tumours, and pressure sores. Detail is provided on managing these conditions, including information on appropriate dressings and pharmacological treatment.

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37

Publications, ICON Health. The Official Patient's Sourcebook on Epidermolysis Bullosa: A Revised and Updated Directory for the Internet Age. Icon Health Publications, 2002.

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