"William T. Schwarz" appeared in Books and Chapters

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"William T. Schwarz" appeared in Books and Chapters

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Book	Author(s)	Year	Publisher
Club men in caricature	William T. Schwarz	1915	Printed by the Roycrofters
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Chapter	Author(s)	Book	Book Authors	Year	Publisher
Integrating User-contributed Geospatial Data with assistive Geotechnology Using a localized Gazetteer	Matthew T. Rice; William C. Hammill; Ahmad O. Aburizaiza; Sara Schwarz; R. Daniel Jacobson	Advances in Cartography and GIScience. Volume 1: Selection from ICC 2011, Paris	Anne Ruas	2011	Springer Berlin Heidelberg
Chapter 54: Subtype selective muscarinic agonists: potential therapeutic agents for Alzheimer's disease	Robert Davis; Charlotte Raby; Michael J. Callahan; William Lipinski; Roy Schwarz; David T. Dudley; David Lauffer; Phillip Reece; Juan Jaen; Haile Tecle	Cholinergic Function and Dysfunction	A. Claudio Cuello	1993	Elsevier
Sect. V. Metabolic Liver Disease. 22. Approach to the Child with Metabolic Liver Disease	Harvey L. Sharp.23.[alpha][subscript 1]-Antitrypsin Deficiency /David H. Perlmutter.24.The Liver and Biliary Tract in Cystic Fibrosis /Kevin J. Gaskin.25.Inborn Errors of Carbohydrate Metabolism /Fayez K. Ghishan and Martha P. Ballew.26.Copper and Iron Storage Disorders /Ronald J. Sokol and Michael R. Narkewicz.27.Neonatal Hemochromatosis /Delphine de Boissieu and A. S. Knisely.28.Porphyrins and Prophyria /Deborah K. Freese.29.Tyrosinemia /Grant A. Mitchell, Pierre A. Russo and Josee Dubois /[et al.].30.The Lysosomal Storage Diseases /Margaret M. McGovern and Pramod K. Mistry.31.Disorders of Bile Acid Synthesis and Metabolism: A Metabolic Basis for Liver Disease /Kenneth D. R. Setchell and Nancy C. O'Connell.32.Inborn Defects in Mitochondrial Fatty Acid Oxidation /William R. Treem.33.Mitochondrial Hepatopathies /Ronald J. Sokol and William R. Treem.34.Peroxisomal Diseases /Paul A. Watkins and Kathleen B. Schwarz.35.Disorders of the Urea Cycle /Michael T. Geraghty and Saul W. Brusilow	Liver disease in children /	Suchy, Frederick J.; Sokol, Ronald J.; Balistreri, William F.	[2001], ©2001.	Lippincott Williams & Wilkins,
"Daddy"	Sylvia Plath; Daniel's story / Carol Matas; "Death fugue" / Paul Celan; The deputy / Rolf Hochhuth; The destruction of the European Jews / Raul Hilberg; The diary of a young girl / Anne Frank; The double bond / Carole Angier; The drowned; the saved / Primo Levi; Eichmann in Jerusalem / Hannah Arendt; "Elegy for N.N." / Czesław Miłosz; Enemies / Isaac Bashevis Singer; Europe Central / William T. Vollmann; Explaining Hitler / Ron Rosenbaum; The fall of France / Julian Jackson; Fateless / Imre Kertész; The fifth son / Elie Wiesel; Friedrich / Hans Peter Richter; The gates of the forest / Elie Wiesel; Ghetto / Joshua Sobol; God's presence in history / Emil L. Fackenheim; Gone to soldiers / Marge Piercy; The hiding place / Corrie ten Boom with John; Elizabeth Sherrill; The history of love / Nicole Krauss; History on trial / Deborah E. Lipstadt; Hitler / Ian Kershaw; The Hitler of history / John Lukacs; Hitler's willing executioners / Daniel Jonah Goldhagen; The Holocaust in American life / Peter Novick; Holocaust politics / John K. Roth; Holocaust testimonies / Lawrence L. Langer; House of dolls / Ka-tzetnik 135633; I will bear witness / Victor Klemperer; In kindling flame / Linda Atkinson; "In the blue distance" / Nelly Sachs; Incident at Vichy / Arthur Miller; An interrupted life / Etty Hillesum; Into that darkness / Gitta Sereny; Jews / Arthur Hertzberg; Aron Hirt-Manheimer; The journey back / Johanna Reiss; "Journey through the night" / Jakov Lind; The last of the just / André Schwarz-Bart; Lest innocent blood be shed / Philip P. Hallie; Letters; papers from prison / Dietrich Bonhoeffer	Holocaust literature	John K. Roth	2008	Salem Press
Pt. II. Syndromes. 8. X-linked Severe Combined Immunodeficiency	Jennifer M. Puck.9.Severe Combined Immune Deficiency Due to Defects of JAK3 Tyrosine Kinase /Fabio Candotti, Anna Villa and Luigi D. Notarangelo.10.Immunodeficiency Disease Due to Deficiency of Adenosine Deaminase /Rochelle Hirschhorn.11.Immunodeficiency Disease Due to Deficiency of Purine Nucleoside Phosphorylase /William R. A. Osborne and Hans D. Ochs.12.SCID Resulting from Mutations in the Gene Encoding the Protein Tyrosine Kinase ZAP-70 /Melissa E. Elder and Arthur Weiss.13.Recombination Defects /Klaus Schwarz, Luigi D. Notarangelo and Eugenia Spanopoulou [et al.].14.Molecular Basis of Major Histocompatibility Complex Class II Deficiency /Walter Reith, Viktor Steimle and Barbara Lisowska-Grospierre [et al.].15.HLA Class I Deficiencies /Henri de la Salle, Lionel Donato and Jaques Zimmer [et al.].16.CD3 Deficiencies /Jose R. Regueiro, Alberto Pacheco and David Alvarez-Zapata [et al.].17.DiGeorge Syndrome: A Chromosome 22q11.2 Deletion Syndrome /Deborah A. Driscoll and Kathleen E. Sullivan.18.Inherited Interferon [gamma]-Receptor Deficiency /Jean-Laurent Casanova, Melanie Newport and Alain Fischer [et al.].19.X-Linked Lymphoproliferative Disease /Volker Schuster and Hans Wolfgang Kreth.20.CD40 Ligand and the Hyper-IgM Syndrome /Narayanaswamy Ramesh, Raif S. Geha and Luigi D. Notarangelo.21.Genetic Approach to Common Variable Immunodeficiency and IgA Deficiency /Lennart Hammarstrom and C. I. Edvard Smith.22.X-Linked Agammaglobulinemia: A Disease of Btk Tyrosine Kinase /C. I. Edvard Smith and Owen N. Witte.23.Autosomal Recessive Agammaglobulinemia /Mary Ellen Conley.24.The Wiskott-Aldrich Syndrome /Hans D. Ochs and Fred S. Rosen.25.Ataxia-Telangiectasia /Martin F. Lavin and Yosef Shiloh.26.Ataxia-Telangiectasia Variants (Nijmegen Breakage Syndrome) /Rolf-Dieter Wegner, Krystyna H. Chrzanowska and Karl Sperling [et al.].27.The Immunodeficiency of Bloom Syndrome /James German.28.Inherited Disorders with Autoimmunity and Defective Lymphocyte Regulation /Jennifer M. Puck, Stephen E. Straus and Francoise Le Deist [et al.].29.Chronic Granulomatous Disease /Dirk Roos and John T. Curnutte.30.Cell Adhesion and Leukocyte Adhesion Defects /Amos Etzioni and John M. Harlan.31.Chediak-Higashi Syndrome /Richard A. Spritz.32.Genetically Determined Deficiencies of the Complement System /Kathleen E. Sullivan and Jerry A. Winkelstein	Primary immunodeficiency diseases: a molecular and genetic approach /	Ochs, Hans D.,; Smith, C. I. Edvard,; Puck, Jennifer,	1999.	Oxford University Press,
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