"Rett Syndrome" - Books

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Results: 1 to 20 of 107 books (569 items)

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Select item 14589841.

GeneReviews® [Internet].

Adam MP, Bick S, Mirzaa GM, et al., editors.

Seattle (WA): University of Washington, Seattle; 1993-2026.

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Select item 58763542.

Trofinetide (Daybue): Therapeutic area: Rett syndrome: Reimbursement Review [Internet].

Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2026 Jan.

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Select item 44036683.

StatPearls [Internet].

Treasure Island (FL): StatPearls Publishing; 2026 Jan-.

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Select item 46389964.

Pharmacological and non-pharmacological interventions for non-respiratory sleep disturbance in children with neurodisabilities: a systematic review.

Beresford B, McDaid C, Parker A, et al.

Southampton (UK): NIHR Journals Library; 2018 Oct. (Health Technology Assessment, No. 22.60.)

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Select item 57048765.

Jasper's Basic Mechanisms of the Epilepsies. 5th edition.

Noebels JL, Avoli M, Rogawski MA, et al., editors.

New York: Oxford University Press; 2024.

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Select item 40865006.

Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder [Internet].

Sun F, Oristaglio J, Levy SE, et al.

Rockville (MD): Agency for Healthcare Research and Quality (US); 2015 Jun. (Technical Briefs, No. 23.)

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Select item 29807927.

Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].

Borgaonkar DS.

Bethesda (MD): National Center for Biotechnology Information (US); 1975-.

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Select item 43764988.

Cerebral palsy in under 25s: assessment and management.

National Guideline Alliance (UK).

London: National Institute for Health and Care Excellence (NICE); 2017 Jan. (NICE Guideline, No. 62.)

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Select item 23871569.

Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition.

Noebels JL, Avoli M, Rogawski MA, et al., editors.

Bethesda (MD): National Center for Biotechnology Information (US); 2012.

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Select item 581903410.

Trofinetide (Daybue): Indication: For the treatment of Rett syndrome in adults and pediatric patients 2 years of age and older and weighing at least 9 kg: Reimbursement Recommendation [Internet].

Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2025 Aug.

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Select item 491624611.

NTP Research Report on Systematic Literature Review on the Effects of Fluoride on Learning and Memory in Animal Studies: Research Report 1 [Internet].

National Toxicology Program.

Research Triangle Park (NC): National Toxicology Program; 2016 Jul.

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Select item 251951812.

Rare Diseases and Orphan Products: Accelerating Research and Development.

Institute of Medicine (US) Committee on Accelerating Rare Diseases Research and Orphan Product Development; Field MJ, Boat TF, editors.

Washington (DC): National Academies Press (US); 2010.

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Select item 516880213.

Respite care and short breaks for young adults aged 18–40 with complex health-care needs: mixed-methods systematic review and conceptual framework development.

Knighting K, Pilkington G, Noyes J, et al.

Southampton (UK): NIHR Journals Library; 2021 Feb. (Health Services and Delivery Research, No. 9.6.)

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Select item 432377414.

Mental Health Problems in People with Learning Disabilities: Prevention, Assessment and Management.

National Guideline Alliance (UK).

London: National Institute for Health and Care Excellence (NICE); 2016 Sep. (NICE Guideline, No. 54.)

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Select item 409165415.

Challenging Behaviour and Learning Disabilities: Prevention and Interventions for People with Learning Disabilities Whose Behaviour Challenges.

National Collaborating Centre for Mental Health (UK).

London: National Institute for Health and Care Excellence (NICE); 2015 May. (NICE Guideline, No. 11.)

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Select item 340129416.

Endotext [Internet].

Feingold KR, Adler RA, Ahmed SF, et al., editors.

South Dartmouth (MA): MDText.com, Inc.; 2000-.

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Select item 562148217.

Melatonin for the Treatment of Insomnia in Children and Adolescents: Rapid Review [Internet].

Tran K, Mahood Q; Authors.

Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2022 Jun.

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Select item 436844218.

Researching outcomes from forensic services for people with intellectual or developmental disabilities: a systematic review, evidence synthesis and expert and patient/carer consultation.

Morrissey C, Geach N, Alexander R, et al.

Southampton (UK): NIHR Journals Library; 2017 Jan. (Health Services and Delivery Research, No. 5.3.)

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Select item 442838619.

First- and Second-Generation Antipsychotics in Children and Young Adults: Systematic Review Update [Internet].

Pillay J, Boylan K, Carrey N, et al.

Rockville (MD): Agency for Healthcare Research and Quality (US); 2017 Mar. (Comparative Effectiveness Reviews, No. 184.)

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Select item 572909020.

Exploring and Exploiting Genetic Risk for Psychiatric Disorders [Internet].

Gordon JA, Binder EB, editors.

Cambridge (MA): MIT Press; 2023.

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Rett Syndrome Types. RTT is diagnosed clinically. Clinical features are divided into typical and atypical presentations. Contributed by G Chahil, MD

Rett Syndrome.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-.
FIGURE 4-1Plot of NIH grants for illustrative rare diseases by disease prevalence

NOTE: Prevalence figures come from Orphanet, 2009 (see discussion of data in Chapter 2). Grant numbers include American Recovery and Reinvestment Act grant supplements and training grants.
SOURCE: NIH Reporter (http://projectreporter.nih.gov/reporter.cfm). ProgeriaNiemann-Pick diseaseFanconi anemiaEhlers-Danlos syndrome (classic)Primary ciliary dyskinesiaRett syndromeDuchenne muscular dystrophyHuntington diseaseTuberous sclerosisLeber congenital amaurosisSickle cell anemiaCystic fibrosisAcute myeloid leukemiaCongenital diaphragmatic herniaSarcoidosisFamilial dilated cardiomyopathyHereditary spherocytosisTurner syndromeGastric cancerNeurofibromatosis (type 1)Alpha₁-antitrypsinMarfan syndromeAmyloidosisA cute respiratory distress syndrome (adult)CryptosporidiosisNon-Hodgkin lymphoma Albright hereditary osteodystrophySclerodermaTetralogy of FallotNarcolepsy (cataplexy)Melanocortin-4 receptor deficiencyNoonan syndrome

Discovery Research for Rare Diseases and Orphan Product Development.

Institute of Medicine (US) Committee on Accelerating Rare Diseases Research and Orphan Product Development; Field MJ, Boat TF, editors. Rare Diseases and Orphan Products: Accelerating Research and Development. Washington (DC): National Academies Press (US); 2010.