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Livros sobre o tema "Cockayne, Syndrome de – Étiologie"

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Autor: Grafiati

Publicado: 25 de maio de 2024

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1

I, Ahmad Shamim, ed. Molecular mechanisms of Cockayne syndrome. Austin, Tex: Landes Bioscience, 2009.

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2

Parker, James N., e Philip M. Parker. Cockayne syndrome: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. San Diego, CA: ICON Health Publications, 2007.

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3

J, Epstein Charles, e National Down Syndrome Society (U.S.), eds. Etiology and pathogenesis of Down syndrome: Proceedings of the International Down Syndrome Research Conference. New York: Wiley-Liss, 1995.

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4

Cantwell, Alan. AIDS and the doctors of death: An inquiry into the origin of the AIDS epidemic. Los Angeles: Aries Rising Press, 1988.

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5

Cantwell, Alan. AIDS and the doctors of death: An inquiry into the origin of the AIDS epidemic. Los Angeles: Aries Rising Press, 1988.

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6

J, Hassold Terry, e Epstein Charles J, eds. Molecular and cytogenetic studies of non-disjunction: Proceedings of the Fifth Annual National Down Syndrome Society Symposium held in New York, NY, December 1-2, 1988. New York: A.R. Liss, 1989.

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7

L, Petrakis Peter, American Medical Society on Alcoholism and Other Drug Dependencies., National Council on Alcoholism e AIDS and Chemical Dependency Forum (1986 : San Francisco, Calif.), eds. Acquired Immune Deficiency Syndrome and chemical dependency: Report of symposium. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Alcohol Abuse and Alcoholism, 1987.

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8

Mazeau, Michèle. Dysphasies, troubles mnésiques, syndrome frontal chez l'enfant atteint de lésions cérébrales précoces: Du trouble à la rééducation. Paris: Masson, 1999.

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9

Mazeau, Michèle. Dysphasies, troubles mnésiques, syndrome frontal chez l'enfant atteint de lésions cérébrales précoces: Du trouble à la rééducation. Paris: Masson, 1997.

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10

The failed back syndrome: Etiology and therapy. 2^a ed. New York: Springer-Verlag, 1992.

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11

Kristen, Strom Terry, e Fox Barry, eds. Syndrome X: Overcoming the silent killer that can give you a heart attack. New York: Simon and Schuster, 2000.

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12

Schamberger, Wolf. The malalignment syndrome: Implications for medicine and sport. Edinburgh: Churchill Livingstone, 2002.

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13

History of AIDS: Emergence and origin of a modern pandemic. Princeton, N.J: Princeton University Press, 1990.

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14

Toxic exposures: Contested illnesses and the environmental health movement. New York: Columbia University Press, 2007.

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15

Brown, Phil. Toxic exposures: Contested illnesses and the environmental health movement. New York, NY: Columbia University Press, 2007.

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16

Ahmad, Shamim I. Molecular Mechanisms of Cockayne Syndrome. Taylor & Francis Group, 2009.

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17

Ahmad, Shamim I. Molecular Mechanisms of Cockayne Syndrome. Taylor & Francis Group, 2009.

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18

Sybert, Virginia P. Premature Aging. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0012.

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19

Wilkinson, Harold A. Failed Back Syndrome: Etiology and Therapy. Springer London, Limited, 2012.

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20

Wilkinson, Harold A. Failed Back Syndrome: Etiology and Therapy. Springer, 2012.

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21

Sybert, Virginia P. Premature Aging. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0012.

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Chapter 12 covers Cockayne Syndrome, De Barsy Syndrome, Hallermann-Streiff Syndrome, Hutchinson-Gilford Progeria, and Werner Syndrome. 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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22

Wilkinson, Harold A. The Failed Back Syndrome: Etiology and Therapy. Springer, 1991.

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23

Schamberger, Wolf. Malalignment Syndrome: Implications for Medicine and Sport. Elsevier - Health Sciences Division, 2012.

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24

SCHAMBERGER, WOLF. The Malalignment Syndrome: Biomechanical and Clinical Implications for Medicine and Sports. Churchill Livingstone, 2002.

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25

Grmek, Mirko D. History of AIDS. Princeton University Press, 1993.

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26

Schamberger, Wolf. Malalignment Syndrome: Diagnosis and Treating a Common Cause of Acute and Chronic Pelvic, Leg and Back Pain. Elsevier - Health Sciences Division, 2012.

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27

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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28

Brown, Phil. Toxic Exposures. Columbia University Press, 2007.

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29

Brain Fog. Starborn Services, 2000.

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30

AIDS And Drug Misuse Update. Stationery Office Books (TSO), 1993.

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31

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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32

(Editor), Tracie L. Miller, e Sherwood L. Gorbach (Editor), eds. Nutritional Aspects of HIV Infection. A Hodder Arnold Publication, 1999.

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33

Masur, Henry. Respiratory Infections in Patients With HIV. Lippincott Williams & Wilkins, 1999.

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