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Thematische Bibliographien / Pediatric metabolic syndrome / Bücher

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Bücher zum Thema „Pediatric metabolic syndrome“

Autor: Grafiati

Veröffentlicht am 7. Juni 2025

Zuletzt aktualisiert am 2. August 2025

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1

Lipshultz, Steven E., Sarah E. Messiah, and Tracie L. Miller, eds. Pediatric Metabolic Syndrome. Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-2366-8.

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2

Kiess, W., Arya M. Sharma, Martin Wabitsch, and Claudio Maffeis. Metabolic syndrome and obesity in childhood and adolescence. Karger, 2015.

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3

Laboratories, Ross, Brown University, and University of Colorado (System), eds. The micropremie: The next frontier : report of the 99th Ross Conference on Pediatric Research. Ross Laboratories, 1990.

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4

Gilbert, Patricia. The A-Z reference book of syndromes and inheriteddisorders. 2nd ed. Singular Pub. Group, 1996.

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5

Gilbert, Patricia. The A-Z reference book of syndromes and inherited disorders: A manual for health, social, and education workers. Chapman & Hall, 1993.

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6

Cohen, M. Michael. Overgrowth syndromes. Oxford University Press, 2002.

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7

Pediatric Metabolic Syndrome Comprehensive Clinical Review And Related Health Issues. Springer, 2012.

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8

Lipshultz, Steven E., Sarah E. Messiah, and Tracie L. Miller. Pediatric Metabolic Syndrome: Comprehensive Clinical Review and Related Health Issues. Springer London, Limited, 2012.

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9

Lipshultz, Steven E., Sarah E. Messiah, and Tracie L. Miller. Pediatric Metabolic Syndrome: Comprehensive Clinical Review and Related Health Issues. Springer, 2014.

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10

Kamat, Deepak M., Henry M. Adam, and Rebecca A. Baum, eds. Quick Reference Guide to Pediatric Care. 2nd ed. American Academy of Pediatrics, 2017. http://dx.doi.org/10.1542/9781610021128.

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Significantly revised and updated, the second edition of this popular quick reference guide provides information and advice on 190 areas of current pediatric care, everything from abdominal pain and ADHD, to headache and herpes infections, to weight loss and wheezing. This indispensable resource delivers practical, action-orientated, clinical solutions for healthcare professionals to use during or between patient encounters. Authoritative content is presented in a concise outline format that helps speed and simplify decision-making. Regardless of the patient presentation you're confronted with

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11

Kleinman, Ronald E., and Frank R. Greer, eds. Pediatric Nutrition (Sponsored Member Benefit). 7th ed. American Academy of Pediatrics, 2013. http://dx.doi.org/10.1542/9781581108606.

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The new 7th edition provides the latest information about nutrient metabolism and nutrition to support the normal development and health of infants and children who are well, those born with congenital anomalies or disorders of metabolism, and those with acute and chronic illnesses. Contents include: - The latest evidence-based guidelines on feeding healthy infants and children - Current policies and practice recommendations from the AAP Committee on Nutrition - Several new chapters and appendices have been added, including chapters on school and daycare nutrition; gene and nutrient interactio

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12

Meier, Petra M., and Thomas O. Erb. Craniosynostosis and Apert Syndrome. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0021.

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Apert syndrome is a complex, progressive multisystem condition of the craniosynostosis spectrum originating from a fibroblast growth factor receptor disorder. Multidisciplinary treatment teams may include craniofacial surgery, neurosurgery, otolaryngology, ophthalmology, oro-maxillofacial surgery, and pediatric intensive care. Secondary to midface hypoplasia, children often present with a compromised airway and have a high incidence of sleep disorders. Anesthetic considerations include difficult airway assessment, the presence of obstructive sleep apnea syndrome, and increased intracranial pre

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13

Harney, Jacob P., Kathryn Gudsnuk, Ami Patel, Anantha R. Vellipuram, Sathyajit Bandaru, and David Butler. Endocrine and Reproductive Effects of Ketogenic Diets. Edited by Detlev Boison. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190497996.003.0025.

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This chapter reviews endocrine, behavioral, and reproductive outcomes of the ketogenic diet (KD) in rodent mouse and rat models. KD treatment can result in conditions seen in metabolic syndrome, including dyslipidemia and inflammation. Females raised on low protein KDs will experience delayed puberty onset. Results presented suggest an increase in ketones and a decrease in spatial memory as percent protein drops. Postpubertal female pups fed KD experienced similar cognitive decline to KD-fed dams, despite consuming only normal rodent chow since weaning. This finding is consistent with the deve

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14

Baum, Victor C., and Jennifer E. O'Flaherty. Anesthesia for Genetic, Metabolic, and Dysmorphic Syndromes of Childhood. Lippincott Williams & Wilkins, 2015.

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15

Baum, Victor C., and Jennifer E. O'Flaherty. Anesthesia for Genetic, Metabolic, and Dysmorphic Syndromes of Childhood. 2nd ed. Lippincott Williams & Wilkins, 2006.

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16

Pearl, Phillip L., and William P. Welch. Pediatric Neurotransmitter Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0059.

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The pediatric neurotransmitter disorders represent an enlarging group of neurological syndromes characterized by inherited abnormalities of neurotransmitter synthesis, metabolism, and transport. Disorders involving monoamine synthesis include guanosine triphosphate cyclohydrolase deficiency (Segawa disease or classical Dopa-responsive dystonia as the heterozygous form), aromatic amino acid decarboxylase deficiency, tyrosine hydrolase deficiency, sepiapterin reductase deficiency, and disorders of tetrahydrobiopterin synthesis. These disorders can be classified according to whether they feature

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17

Brown, Roy I., and Terrance N. James. Prader-Willi Syndrome: Home, School and Community. Singular Pub Group, 1992.

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18

Gilbert, Patricia. The A-Z Reference Book of Syndromes and Inherited Disorders: A Manual for Health, Social and Education Workers. Singular Pub Group, 1992.

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19

Nass, MD, Ruth, and Yitzchak Frank, MD, eds. Cognitive and Behavioral Abnormalities of Pediatric Diseases. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195342680.001.0001.

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This book provides a detailed account of intellectual, other neuropsychological and behavioral manifestations of general pediatric diseases. The conditions discussed include the whole range of pediatric diseases - genetic syndromes, other congenital conditions, metabolic, endocrine, gastrointestinal, infectious, immunologic, toxic, trauma, and neoplastic, as well as sensory disabilities including deafness and blindness. Although the book is not intended to discuss cognitive and behavioral manifestations of conditions usually considered to be primary neurological disease, some of those, includi

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20

Jr, Cohen M. Michael, Giovanni Neri, and Rosanna Weksberg. Overgrowth Syndromes. Oxford University Press, 2001.

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21

Neri, Giovanni, Roger E. Stevenson, and Luigi Bocutto. Overgrowth Syndromes: A Clinical Guide. Oxford University Press, Incorporated, 2019.

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22

Holland-Hall, Cynthia, and Paula K. Braverman, eds. AM:STARs: Hot Topics in Adolescent Health, Vol. 25, No. 2. American Academy of Pediatrics, 2014. http://dx.doi.org/10.1542/9781581108910.

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This issue of AM:STARs, Hot Topics in Adolescent Health, presents a wide array of articles exploring some of the most exciting advances and controversies in adolescent health. These topics and other evolving areas are presented to guide the reader toward providing state of the art clinical care to adolescents, as well as reviewing new research that will shape the future of adolescent health. Topics include: Nutritional and metabolic controversies including the diagnosis of gluten intolerance, vitamin D deficiency and metabolic syndrome in adolescents, and the use of bariatric surgery to treat

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