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Understanding relationships between autism, intelligence, and epilepsy: a cross-disorder approach.
Dev Med Child Neurol. 2013 Feb;55(2):146-153. doi: 10.1111/dmcn.12044. Epub 2012 Dec 4.
Dev Med Child Neurol. 2013.
PMID: 23205844
Free PMC article.
Emotional functioning of patients with neurofibromatosis tumor suppressor syndrome.
Wang DL, Smith KB, Esparza S, Leigh FA, Muzikansky A, Park ER, Plotkin SR.
Wang DL, et al. Among authors: leigh fa.
Genet Med. 2012 Dec;14(12):977-82. doi: 10.1038/gim.2012.85. Epub 2012 Aug 9.
Genet Med. 2012.
PMID: 22878510
Free PMC article.
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Current whole-body MRI applications in the neurofibromatoses: NF1, NF2, and schwannomatosis.
Ahlawat S, Fayad LM, Khan MS, Bredella MA, Harris GJ, Evans DG, Farschtschi S, Jacobs MA, Chhabra A, Salamon JM, Wenzel R, Mautner VF, Dombi E, Cai W, Plotkin SR, Blakeley JO; Whole Body MRI Committee for the REiNS International Collaboration; REiNS International Collaboration Members 2016.
Ahlawat S, et al.
Neurology. 2016 Aug 16;87(7 Suppl 1):S31-9. doi: 10.1212/WNL.0000000000002929.
Neurology. 2016.
PMID: 27527647
Free PMC article.
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Developing multidisciplinary clinics for neuromuscular care and research.
Paganoni S, Nicholson K, Leigh F, Swoboda K, Chad D, Drake K, Haley K, Cudkowicz M, Berry JD.
Paganoni S, et al.
Muscle Nerve. 2017 Nov;56(5):848-858. doi: 10.1002/mus.25725. Epub 2017 Aug 29.
Muscle Nerve. 2017.
PMID: 28632945
Free PMC article.
Review.
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Neurology Care, Diagnostics, and Emerging Therapies of the Patient With Duchenne Muscular Dystrophy.
Leigh F, Ferlini A, Biggar D, Bushby K, Finkel R, Morgenroth LP, Wagner KR.
Leigh F, et al.
Pediatrics. 2018 Oct;142(Suppl 2):S5-S16. doi: 10.1542/peds.2018-0333C.
Pediatrics. 2018.
PMID: 30275245
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Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
Johnson JO, Chia R, Miller DE, Li R, Kumaran R, Abramzon Y, Alahmady N, Renton AE, Topp SD, Gibbs JR, Cookson MR, Sabir MS, Dalgard CL, Troakes C, Jones AR, Shatunov A, Iacoangeli A, Al Khleifat A, Ticozzi N, Silani V, Gellera C, Blair IP, Dobson-Stone C, Kwok JB, Bonkowski ES, Palvadeau R, Tienari PJ, Morrison KE, Shaw PJ, Al-Chalabi A, Brown RH Jr, Calvo A, Mora G, Al-Saif H, Gotkine M, Leigh F, Chang IJ, Perlman SJ, Glass I, Scott AI, Shaw CE, Basak AN, Landers JE, Chiò A, Crawford TO, Smith BN, Traynor BJ; FALS Sequencing Consortium; American Genome Center; International ALS Genomics Consortium; and ITALSGEN Consortium; Smith BN, Ticozzi N, Fallini C, Gkazi AS, Topp SD, Scotter EL, Kenna KP, Keagle P, Tiloca C, Vance C, Troakes C, Colombrita C, King A, Pensato V, Castellotti B, Baas F, Ten Asbroek ALMA, McKenna-Yasek D, McLaughlin RL, Polak M, Asress S, Esteban-Pérez J, Stevic Z, D'Alfonso S, Mazzini L, Comi GP, Del Bo R, Ceroni M, Gagliardi S, Querin G, Bertolin C, van Rheenen W, Rademakers R, van Blitterswijk M, Lauria G, Duga S, Corti S, Cereda C, Corrado L, Sorarù G, Williams KL, Nicholson GA, Blair IP, Leblond-Manry C, Rouleau GA, Hardiman O, Morrison KE, Veldink JH, van …
See abstract for full author list ➔
Johnson JO, et al.
JAMA Neurol. 2021 Oct 1;78(10):1236-1248. doi: 10.1001/jamaneurol.2021.2598.
JAMA Neurol. 2021.
PMID: 34459874
Free PMC article.
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Optical coherence tomography in the evaluation of neurofibromatosis type-1 subjects with optic pathway gliomas.
Chang L, El-Dairi MA, Frempong TA, Burner EL, Bhatti MT, Young TL, Leigh F.
Chang L, et al.
J AAPOS. 2010 Dec;14(6):511-7. doi: 10.1016/j.jaapos.2010.08.014.
J AAPOS. 2010.
PMID: 21168074
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Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume.
Waldau B, Domeshek LF, Leigh FA, Lum KC, Fuchs HE, Marcus JR, Mukundan S, Grant GA.
Waldau B, et al. Among authors: leigh fa.
J Neurosurg Pediatr. 2009 Feb;3(2):110-4. doi: 10.3171/2008.10.PEDS08200.
J Neurosurg Pediatr. 2009.
PMID: 19278309
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