The Ehlers‐Danlos Syndrome

Cited by (360)

Items 201–300 of 360

1. Aspects on dental hard tissues in primary teeth from patients with Ehlers–Danlos syndrome
   Gunilla Klingberg, Catharina Hagberg, Jörgen G. Norén, Sándor Nietzsche · 2009 · International Journal of Paediatric Dentistry
2. Orthodontic treatment protocol of Ehlers-Danlos syndrome type VI.
   Tülin Arun, Didem Nalbantgil, Korkmaz Sayınsu · 2006 · PubMed
3. Ehlers—Danlos syndrome and multiple sclerosis: a possible association
   Janek Vilisaar, Sreedharan Harikrishnan, Mohnish Suri, Cris S. Constantinescu · 2008 · Multiple Sclerosis Journal
4. Arthralgias, fatigue, paresthesias and visceral pain: can joint hypermobility solve the puzzle? A case report
   Marco Folci, FRANCO CAPSONI · 2016 · BMC Musculoskeletal Disorders
5. Correlation between Oral Health-Related Quality of Life and Objectively Measured Oral Health in People with Ehlers–Danlos Syndromes
   Ole Oelerich, Johannes Kleinheinz, Daniel Ralph Reissmann, Jeanette Köppe, Marcel René Hanisch · 2020 · International Journal of Environmental Research and Public Health
6. Prevalence and quality of temporomandibular disorders, chronic pain and psychological distress in patients with classical and hypermobile Ehlers-Danlos syndrome: an exploratory study
   Willich, Leon, Bohner, Lauren, Köppe, Jeanette, Jackowski, Jochen, Hanisch, Marcel, Oelerich, Ole · 2023 · Orphanet Journal of Rare Diseases
7. Suicidal Behaviors in Women With the Hypermobile Ehlers–Danlos Syndrome
   Carolina Baeza‐Velasco, C. Hamonet, Lucile Montalescot, Philippe Courtet · 2021 · Archives of Suicide Research
8. Schweizer Warmblutfohlen mit Symptomen von hereditärer dermaler Asthenie (HERDA) ohne Mutation im Cyclophilin B-Gen (PPIB)
   Silvia Rüfenacht, R. Straub, Beat U. Steinmann, Nena J. Winand, A. Bidaut, Michael Hubert Stoffel, Vincent Gerber, Marianne Wyder, Eliane J. Müller, J. P. Roosje · 2010 · Schweizer Archiv für Tierheilkunde
9. Audit of Gastrointestinal Manifestations in Patients with Loeys–Dietz Syndrome and Vascular Ehlers–Danlos Syndrome
   Wang, Xiao Jing, Babameto, Mary, Babovic-Vuksanovic, Dusica, Bowen, Juan M., Camilleri, Michael · 2021 · Digestive Diseases and Sciences
10. An overview of Ehlers Danlos syndrome and the link between postural orthostatic tachycardia syndrome and gastrointestinal symptoms with a focus on gastroparesis
    William Ka Kei Wu, Vincent Ho · 2024 · Frontiers in Neurology
11. Non-operative management of diverticular perforation in a patient with suspected Ehlers-Danlos syndrome
    M.C. Casey, I. Robertson, Peadar S. Waters, J Hanaghan, W. Khan, Kevin Barry · 2014 · International Journal of Surgery Case Reports
12. A novel technique to treat traumatic corneal perforation in a case of presumed brittle cornea syndrome
    H M Hussin, S. Biswas, M Majid, R. Haynes, Derek M. Tole · 2007 · British Journal of Ophthalmology
13. Heritable Diseases of Connective Tissue
    Deborah Krakow · 2013 · Elsevier eBooks
14. The multifaceted and complex hypermobility syndrome (a.k.a. Ehlers-Danlos Syndrome Hypermobility Type): evaluation and management through a rehabilitative approach.
    Claudia Celletti, Filippo Camerota · 2013 · PubMed
15. L-proline determination by molecularly imprinted nanoparticles: A potential nanoscale tool for the diagnosis of metabolic disorders
    Mustafa Nergiz, Okan Zenger, Gözde Baydemir · 2024 · Journal of Chromatography A
16. Discovery and Delineation of Dermatan 4-O-Sulfotransferase-1 (D4ST1)-Deficient Ehlers-Danlos Syndrome
    Kosho, Tomoki · 2013 · Current Genetics in Dermatology
17. Foot Type Analysis Based on Electronic Pedobarography Data in Individuals with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type During Upright Standing
    Verônica Cimolin, Manuela Galli, Claudia Celletti, Massimiliano Pau, Marco Castori, Gianfranco Morico, Giorgio Albertini, Filippo Camerota · 2014 · Journal of the American Podiatric Medical Association
18. Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers–Danlos syndrome with severe intestinal involvement: a case report
    Francesca Cortini, Barbara Marinelli, Manuela Seia, Barbara De Giorgio, Angela Cecilia Pesatori, Nicola Montano, Alessandra Bassotti · 2016 · Journal of Medical Case Reports
19. Pathophysiology of Acute Aortic Syndromes
    Christoph Anton Nienaber · 2007 · Springer eBooks
20. Abnormal Retinal Blood Vessels in Ehlers-Danlos Syndrome Type VI
    Nobuhiko Chikamoto, Shinichiro Teranishi, Tai-ichiro Chikama, Teruo Nishida, Kenji Ohshima, Yoshikazu Hatsukawa · 2007 · Japanese Journal of Ophthalmology
21. Collagen Dysregulation in the Dermis of the Sagg/+ Mouse: A Loose Skin Model
    Paul J. Christner, Julieta Gentiletti, Josephine Peters, Simon T. Ball, Mitsuo Yamauchi, Phimon Atsawasuwan, David P. Beason, Louis J. Soslowsky, David E. Birk · 2006 · Journal of Investigative Dermatology
22. Hypermobility syndromes from the clinician's perspective: an overview.
    Johannes W. G. Jacobs, José António Pereira da Silva · 2014 · PubMed
23. Ehlers-Danlos Syndrome in Athletes
    Erik L. Schroeder, Mark E. Lavallee · 2006 · Current Sports Medicine Reports
24. Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene
    L.C. Walker, Ahmad Said Teebi, Joan C. Marini, Anne De Paepe, Fransiska Malfait, Phimon Atsawasuwan, M. Yamauchi, Heather N. Yeowell · 2004 · Molecular Genetics and Metabolism
25. Ehlers-Danlos syndrome.
    Ben C.J. Hamel · 2004 · PubMed
26. Ehlers–Danlos Syndromes
    Nigel Burrows · 2019 · Wiley eBooks
27. Macronodular adrenocortical hyperplasia in a postmenopausal woman.
    G. Sophie Mijnhout, Sven A. Danner, Frank R.W. van de Goot, Eveline W. C. M. van Dam · 2004 · PubMed
28. Novel mutation in theCHST14gene causing musculocontractural type of Ehlers-Danlos syndrome
    Sapna Sandal, Anupriya Kaur, Inusha Panigrahi · 2018 · BMJ Case Reports
29. Substrate specificity of lysyl hydroxylase isoforms and multifunctionality of lysyl hydroxylase 3
    Maija Risteli · 2008
30. Differential diagnosis of muscular hypotonia in infants: The kyphoscoliotic type of Ehlers–Danlos syndrome (EDS VI)
    Nicol Cornelia Voermans, Baziel G.M. van Engelen · 2008 · Neuromuscular Disorders
31. Constructing networks for comparison of collagen types
    Wesp, Valentin, Scholz, Lukas, Ziermann-Canabarro, Janine M., Schuster, Stefan, Stark, Heiko · 2024 · Journal of Integrative Bioinformatics
32. Spontaneous Rupture of an Aneurysm of the Right Subclavian Artery as a First Presentation of Ehlers Danlos Syndrome in a 15-year Old Boy
    Ans Verbert, Jürgen Verbist, Patrick Peeters, H. Deferm, L. Haenen · 2013 · Acta chirurgica Belgica
33. Ehlers–Danlos syndrome: A cause of epilepsy and periventricular heterotopia
    Alberto Verrotti, Debora Monacelli, Miriam Castagnino, Maria Pia Villa, Pasquale Parisi · 2014 · Seizure
34. Ehlers–Danlos Syndrome
    Fransiska Malfait, Anne De Paepe · 2013 · Elsevier eBooks
35. Mobile Cecum in a Young Woman with Ehlers-Danlos Syndrome Hypermobility type: A Case Report and Review of the Literature
    Fukuda, Yoshihisa, Higuchi, Yusuke, Shinozaki, Kanae, Tanigawa, Yuji, Abe, Taro, Hanaoka, Nobuyoshi, Matsubayashi, Sunao, Yamaguchi, Tomomi, Kosho, Tomoki, Nakamichi, Koji · 2017 · Internal Medicine
36. Ehlers-Danlos syndrome type VI in a 17-year-old Iranian boy with severe muscular weakness – a diagnostic challenge?
    Ariana Kariminejad, Bita Bozorgmehr, Alireza Khatami, Mohamad Hasan Kariminejad, Cecilia Giunta, Beat U. Steinmann · 2010 · Europe PMC (PubMed Central)
37. Concurrent Splenic Peliosis and Vascular Ehlers-Danlos Syndrome
    Arianne C. van Bon, Jón Kristinsson, J.H.J.M. van Krieken, Geert J. A. Wanten · 2008 · Annals of Vascular Surgery
38. Morphometric analysis of thoracic aorta in Slc39a13/Zip13-KO mice
    Takuya Hirose, Takamasa Shimazaki, Naoki Takahashi, Toshiyuki Fukada, Takafumi Watanabe, Prasarn Tangkawattana, Kazushige TAKEHANA · 2019 · Cell and Tissue Research
39. Collagen and Bleeding Diathesis in Ehlers‐Danlos Syndrome
    Alf Udén · 1982 · Scandinavian Journal of Haematology
40. Amino Acid Pairs Sensitive to Variants in Human Collagen alpha1(I) Chain Precursor
    Guang Wu, Shaomin Yan · 2004 · Technische Universität Dortmund Eldorado (Technische Universität Dortmund)
41. Expression of lysyl hydroxylases and characterization of a novel disorder caused by mutations in the lysyl hydroxylase 3 gene
    Antti M. Salo · 2009
42. On the role of the glycosylation of type I collagen in bone
    Luco Rutten, Elena Macías‐Sánchez, Nico A. J. M. Sommerdijk · 2024 · Journal of Structural Biology
43. Ehlers-Danlos Syndromes
    Salvatore Savasta, Maurizia Valli · 2008 · Springer eBooks
44. Clinical utility gene card for: Ehlers–Danlos syndrome types I–VII
    Karin Mayer, Ingo Kennerknecht, Beat U. Steinmann · 2010 · European Journal of Human Genetics
45. Pathological Case of the Month
    Christof Dame, Ingrid Haußer, Janique Geukens, Rolf Erwin Brenner · 2001 · Archives of Pediatrics and Adolescent Medicine
46. Case Report: Identification and Functional Analysis of a Homozygous Synonymous Variant in the PLOD1 Gene in a Chinese Neonatal With the Ehlers–Danlos Syndrome
    Xiaodan Yan, Jianbo Shu, Yanyan Nie, Ying Zhang, Ping Wang, Weiwei Zhou, Xiaoyu Cui, Yang Liu · 2022 · Frontiers in Pediatrics
47. The Relationship Between Fatigue, Pain Interference, Pain-Related Distress, and Avoidance in Pediatric Hypermobile Ehlers–Danlos Syndrome
    Olivia E. Sokol, Emma E. Biggs, Ardin S. Berger, Laura E. Simons, Rashmi Parekh Bhandari · 2025 · Children
48. Evaluating the effects of two different kinesiology taping techniques on shoulder pain and function in patients with hypermobile Ehlers-Danlos syndrome
    Frank T. Tudini, David F. Levine, Michael Healy, Max Jordon, Kevin K. Chui · 2023 · Frontiers in Pain Research
49. Collagen V haploinsufficiency in female murine patellar tendons results in altered matrix engagement and cellular density, demonstrating decreased healing
    Jaclyn A. Carlson, Snehal S. Shetye, Mei Sun, Stephanie N. Weiss, David E. Birk, Louis J. Soslowsky · 2023 · Journal of Orthopaedic Research®
50. Ehlers–Danlos Syndrome
    Peter H. Byers · 2013 · Elsevier eBooks
51. Patient interest in the development of a center for Ehlers-Danlos syndrome/hypermobility spectrum disorder in the Chicagoland region
    Wendy Wagner, Tom A. Doyle, Clair A. Francomano, Dacre R. T. Knight, Colin Michael Egenberger Halverson · 2024 · Orphanet Journal of Rare Diseases
52. Comorbidities and neurosurgical interventions in a cohort with connective tissue disorders
    Ilene S. Ruhoy, Paolo A. Bolognese, Jared S. Rosenblum, Randall A. Dass, Navdeep S. Nayyer, Jeffrey D. Wood, John B. Biggins · 2025 · Frontiers in Neurology
53. Surgical treatment of abdominal wall weakness and lumbar hernias in Ehlers-Danlos syndrome – Case report
    Oliver Scheufler, Julian Ramin Andresen, Reimer Andresen · 2020 · International Journal of Surgery Case Reports
54. Wound Repair Capability in EDS Fibroblasts can be Retrieved by Exogenous Type V Collagen
    Simona Viglio, Nicoletta Zoppi, Antonella Sangalli, Angelo Gallanti, Sergio Barlati, Monica Mottes, Marina Colombi, Maurizia Valli · 2008 · The Scientific World JOURNAL
55. Classic Ehlers-Danlos syndrome: case report and brief review of literature.
    Paulo Morais, Olga Ferreira, Sofia Magina, Cármen Silva, Miguel Leão, Ana Maria Maia, Filomena Azevedo · 2013 · PubMed
56. Increased augmentation index in patients with Ehlers-Danlos syndrome
    Maurice Roeder, Sira Thiel, Frédéric Baumann, Noriane Andrina Sievi, Marianne Rohrbach, Malcolm Kohler, Thomas Gaisl · 2020 · BMC Cardiovascular Disorders
57. An unequal crossover event in RCCX modules of the human MHC resulting in the formation of a TNXB/TNXA hybrid and deletion of the CYP21A
    Taina Jaatinen, Erwin K. Chung, Olli Ruuskanen, Marja‐Liisa Lokki · 2002 · Human Immunology
58. Lumbar artificial disc replacement in Ehlers-Danlos syndrome: A case report and discussion of clinical management
    Emily M. Lindley, Brianna N. Patti, Matthew R. Taylor, Evalina L. Burger, Vikas V. Patel · 2012 · The International Journal of Spine Surgery
59. HERITABLE COLLAGEN DISORDERS: FROM GENOTYPE TO PHENOTYPE
    Anne De Paepe, Lieve Nuytinck · 2001 · Acta Clinica Belgica
60. Ehlers–Danlos Syndromes
    Nigel Burrows, Navjeet Sidhu‐Malik, Heather N. Yeowell · 2011 · Wiley eBooks
61. Genetics of the Ehlers–Danlos syndrome: More than collagen disorders
    Van Damme, Tim, Syx, Delfien, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Malfait, Fransiska · 2015 · Expert Opinion on Orphan Drugs
62. Stroke in Ehlers-Danlos Syndrome Kyphoscoliotic Type: Dissection or Vasculitis?
    Annegret Barbara Quade, Martin Wiesmann, Joachim Weis, Ingo Kurth, Houman Jalaie, Marianne Rohrbach, Martin Häusler · 2017 · Pediatric Neurology
63. A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
    Rosaura Conti, Chiara Zanchi, Egidio Barbi · 2021 · The Italian Journal of Pediatrics/Italian journal of pediatrics
64. A novel variant in the DSE gene leads to Ehlers–Danlos musculocontractural type 2 in a Pakistani family
    Ikram Ullah, Muhammad Aamir, Muhammad Ilyas, Akmal Ahmed, Musharraf Jelani, Wahid Ullah, Muhammad Abbas, Muhammad Ishfaq, Fawad Ali, Janice Yip et al. · 2021 · Congenital Anomalies
65. Stretched beyond the limit : Well-being and functioning in patients with Ehlers-Danlos syndrome and other hypermobility syndromes
    Rinie Geenen, Lumley · 2018 · Utrecht University Repository (Utrecht University)
66. Proximal paraparesis due to aortic dissection extending into bilateral carotid arteries in a patient with Loeys-Dietz syndrome
    Christopher Goshgarian, ANA H BONETTI LUGO, Richard Salazar · 2013 · Journal of Clinical Neuroscience
67. Congenital Keratoglobus with Multiple Cardiac Anomalies: A Case Presentation and Literature Review
    Pinar Altıaylık Özer, Züleyha Yalnız-Akkaya · 2014 · Seminars in Ophthalmology
68. DUP25 remains unconfirmed
    Stefan J. T. Vermeulen, Björn Menten, Sylvia De Bie, Paul J. Coucke, Bart Loeys, Fransiska Malfait, Julie F A De Backer, Frank Speleman, Anne De Paepe · 2004 · American Journal of Medical Genetics Part A
69. Vascular haemostasis
    Nigel S. Key, Anne De Paepe, Fransiska Malfait, Claire L. Shovlin · 2010 · Haemophilia
70. From the bedside to the bench and backwards: diagnostic approach and management of Ehlers-Danlos syndrome(s) in Italy
    Marco Castori, Marina Colombi · 2015 · Journal de Réadaptation Médicale Pratique et Formation en Médecine Physique et de Réadaptation
71. Ehlers-Danlos syndrome: a review
    Samina Nayani, Joanna Dick, Charlotte Curl · 2019 · Dental Update
72. Ehlers Danlos Syndrome with Glycosaminoglycan Abnormalities
    Noriko Miyake, Tomoki Kosho, Naomichi Matsumoto · 2021 · Advances in experimental medicine and biology
73. Hypermobile Ehlers-Danlos Syndrome: Caregiver–Child Concordance Across Challenges, Readiness to Change, and Coping
    Keely H. Bieniak, Marissa L. Koven, Helen Bedree, Brad T. Tinkle, Susan T. Tran · 2021 · Clinical Practice in Pediatric Psychology
74. The role of the dental practitioner in diagnosing connective tissue and other systemic disorders: a case report of a patient diagnosed with type III E hlers– D anlos syndrome
    Danyal Hazra Awal, Tim Lloyd, Helen J. Petersen · 2014 · Oral Surgery
75. Aortenruptur bei einem 18-jährigen Mann Postmortale Diagnose eines Ehlers-Danlos-Syndroms Typ IV
    Sibylle Banaschak, Frank Driever, Michael L. Nerlich, Burkhard Madea · 2002 · Rechtsmedizin
76. Dental Considerations in Ehlers-Danlos Syndrome: A Case Report
    Ghassem Ansari, Masoud Fallahinejad Ghajari, Bahareh Nazemi, Behnaz Erfanian · 2015 · Journal of Comprehensive Pediatrics
77. Geschlechtsspezifische Unterschiede in der Gefäßchirurgie
    Andreas Sebastian Peters, Carola Marie Hoffmann-Wieker, Maani Hakimi, Dittmar Böckler · 2012 · Gefässchirurgie
78. ECM-Related Myopathies and Muscular Dystrophies
    Carsten G. Bönnemann, Nicol Cornelia Voermans · 2012 · Elsevier eBooks
79. Changes in skin structure of the Zip13-KO mouse by Makomo (Zizania latifolia) feeding
    Yamauchi Takeshi, Takuya Hirose, Kaho Sato, Kenji Iwai, Naoki Takahashi, Jun A. MINAGUCHI, Takeshi UENO, Prasarn Tangkawattana, Kazushige TAKEHANA · 2017 · Journal of Veterinary Medical Science
80. Ehlers–Danlos Syndrome
    Anne De Paepe, Paul J. Coucke, Fransiska Malfait · 2004 · Informa Healthcare eBooks
81. Ehlers–Danlos Syndrome
    2004 · CRC Press eBooks
82. Association Between Orthostatic Intolerance Symptoms and Cognitive Complaints in Hypermobile Ehlers-Danlos Syndrome (hEDS) and Joint Hypermobility Spectrum Disorder (JHSD): A Cross-Sectional Analysis
    Ansa Tariq, Marium Nadeem Khan, Ayesha Ghazal Jamali, Manaal Amir Basra, Aakash Mahato, Syed Mariyum Imran, Zainab Mohsin, Shivam Singla, Imran K Mirani, Uzma Asmat et al. · 2025 · Cureus
83. A Case of Early Osteoarthritis in a Patient With Ehlers-Danlos Syndrome
    Sydney Tran, Radhika Thakkar, Monica Gillie, Jeffrey Anderson · 2022 · Cureus
84. Development of a convenient peptide‐based assay for lysyl hydroxylase
    Mare Čudić, Deepak A. Patel, Janelle L. Lauer‐Fields, Keith Brew, Gregg Fields · 2007 · Biopolymers
85. Felix Mendelssohn's family's brain condition
    Tomislav Breitenfeld, Drako Breitenfeld, Hansjörg Bäzner · 2019 · The Lancet Neurology
86. Classification, nosology and diagnostics of Ehlers-Danlos syndrome
    Ben C.J. Hamel · 2019 · Journal of Biomedicine and Translational Research
87. Ehlers-Danlos syndrome type IV with gastric adenocarcinoma.
    Rajyani Kanechorn Na Ayuthaya, Nonthaya Patthamapasphong, Thanyachai Sura, Nucha Niumpradit, Objoon Trachoo · 2008 · PubMed
88. Ehlers-Danlos Syndrome Type VIII-A Case Report
    Yufei Chen, Shiao‐Pieng Lee, Cheng-Ping Yu, Chien‐Ping Chiang · 2006 · Dermatologica Sinica
89. Nutritional Supplementation in Ehlers-Danlos Syndrome
    Marco Castori, Michela Bruschini, Carlo Blundo · 2014 · Elsevier eBooks
90. Ehler Danlos Syndrome: An Overview
    Nimisha Kakadia, Niranjan Kanaki · 2011 · Journal of chemical and pharmaceutical research
91. Family with Ehlers–Danlos syndrome (combined classic and vascular type) with rare presentation of progressive myopathy and unusual association of severe facial and trigeminal motor weakness
    Atchayaram Nalini, N Devaraddi, Narayanappa Gayathri, Chandrajit Prasad, Veeramani Preethish‐Kumar, Kiran Polavarapu, Shubham Shantanu · 2017 · Neurology India
92. Gastrointestinal Manifestations of Hypermobile Ehlers-Danlos Syndrome and Dietary Approaches Related to Their Management
    Lauren Steiner, Anne Bodensteiner, Nathaniel Johnson · 2023 · Journal of Orthopedic Research and Therapy
93. Disorders of Connective Tissue
    Chathurarya Siriwardena · 2020 · Springer eBooks
94. Dermatologic, Orthopedic, and Cardiovascular Manifestations and Management in a Geriatric Patient With Dermatosparaxis-Type Ehlers-Danlos Syndrome: A Case Report
    Assem Al Sayed, Chrystal Sumrall · 2024 · Cureus
95. Survival of anterior cruciate ligament reconstruction in patients with Ehlers-Danlos syndrome: A comparison with anatomic risk factors in existing literature
    Sebastian Schmidt, Chilan Bou Ghosson Leite, Alexander Bumberger, Domenico Franco, Cale Andrew Jacobs, Lars C. Richardson, Nikolaos K. Paschos, Simon Goertz, Eric M. Berkson, Peter D. Asnis et al. · 2025 · International Orthopaedics
96. A new look at a rare old disease
    Stephen M. Krane · 2008 · IBMS BoneKEy
97. Acute gingival bleeding in Ehlers–Danlos syndrome
    Neha Bansal, Narinder Dev Gupta, Himanshu Trivedi, Sandhya Maheshwari · 2015 · Journal of Oral and Maxillofacial Surgery Medicine and Pathology
98. Progress in Understanding Genetic Contributions in Syndromic and Non-Syndromic Disorders Associated with Congenital, Neuromuscular, and Idiopathic Scoliosis
    Philip F. Giampietro · 2009 · Springer eBooks
99. Ehlers-Danlos Syndrome Type VI: A Case Report
    Mehmet Canpolat, E. Sahin, Fatih Kardaş, Mehmet Köse, Hakan Gümüş, Hüseyin Per, Sefer Kumandaş · 2014 · Turkish Journal of Pediatric Disease
100. Skeletal Dysplasias and Connective Tissue Disorders
     David L. Rimoin, George E. Tiller · 2011 · Avery's Diseases of the Newborn