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Page 1
Mobius Syndrome: A 35-Year Single Institution Experience.
K McClure P, Kilinc E, Oishi S, I Riccio A, A Karol L. K McClure P, et al. J Pediatr Orthop. 2017 Oct/Nov;37(7):e446-e449. doi: 10.1097/BPO.0000000000001009. J Pediatr Orthop. 2017. PMID: 28538051
To date, no large series exist to characterize the orthopaedic manifestations of Mobius syndrome. METHODS: Medical records at a single tertiary pediatric institution were reviewed for all patients diagnosed with Mobius syndrome from January 1, 1980 to …
To date, no large series exist to characterize the orthopaedic manifestations of Mobius syndrome. METHODS: Medical records at …
Can we talk about myoblast fusion?
Dugdale HF, Ochala J. Dugdale HF, et al. Am J Physiol Cell Physiol. 2021 Sep 1;321(3):C504-C506. doi: 10.1152/ajpcell.00187.2021. Epub 2021 Jul 21. Am J Physiol Cell Physiol. 2021. PMID: 34288723 Free article. No abstract available.
Atypical facet of Mobius syndrome: association with facioscapulohumeral muscular dystrophy.
Kolski HK, Leonard NJ, Lemmers RJ, Bamforth JS. Kolski HK, et al. Muscle Nerve. 2008 Apr;37(4):526-9. doi: 10.1002/mus.20941. Muscle Nerve. 2008. PMID: 18059038
We describe a patient with facioscapulohumeral muscular dystrophy (FSHD) associated with Mobius syndrome and congenital ophthalmoplegia. ...
We describe a patient with facioscapulohumeral muscular dystrophy (FSHD) associated with Mobius syndrome and congenital …
Associated syndromes in patients with Pierre Robin Sequence.
Karempelis P, Hagen M, Morrell N, Roby BB. Karempelis P, et al. Int J Pediatr Otorhinolaryngol. 2020 Apr;131:109842. doi: 10.1016/j.ijporl.2019.109842. Epub 2019 Dec 30. Int J Pediatr Otorhinolaryngol. 2020. PMID: 31927149
OBJECTIVES: Classically, Pierre Robin Sequence (PRS) is a triad of micrognathia, glossoptosis, and airway obstruction, although frequently associated with cleft palate. Current literature reports that Stickler syndrome is the most common syndrome associated with PRS …
OBJECTIVES: Classically, Pierre Robin Sequence (PRS) is a triad of micrognathia, glossoptosis, and airway obstruction, although frequently a …
Treatment Approaches for Altered Facial Expression: A Systematic Review in Facioscapulohumeral Muscular Dystrophy and Other Neurological Diseases.
Rasing NB, van de Geest-Buit WA, Chan OYA, Mul K, Lanser A, van Engelen BGM, Erasmus CE, Fischer AH, Ingels KJAO, Post B, Siemann I, Groothuis JT, Voermans NC. Rasing NB, et al. J Neuromuscul Dis. 2024 Mar 21. doi: 10.3233/JND-230213. Online ahead of print. J Neuromuscul Dis. 2024. PMID: 38517799
BACKGROUND: Facial weakness is a key feature of facioscapulohumeral muscular dystrophy (FSHD) and may lead to altered facial expression and subsequent psychosocial impairment. ...OBJECTIVE: We hypothesize that symptomatic treatment options and psychosocial interventions fo …
BACKGROUND: Facial weakness is a key feature of facioscapulohumeral muscular dystrophy (FSHD) and may lead to altered facial expressi …
Mobius syndrome and transposition of the great vessels.
Raroque HG Jr, Hershewe GL, Snyder RD. Raroque HG Jr, et al. Neurology. 1988 Dec;38(12):1894-5. doi: 10.1212/wnl.38.12.1894. Neurology. 1988. PMID: 3194069
A case of Mobius syndrome was associated with transposition of the aorta and pulmonary artery, as well as acheiria. This combination of anomalies supports the hypothesis that Mobius syndrome is caused by an intrapartum insult during the fourth to seven …
A case of Mobius syndrome was associated with transposition of the aorta and pulmonary artery, as well as acheiria. This combi …
The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.
Graeber CP, Hunter DG, Engle EC. Graeber CP, et al. Semin Ophthalmol. 2013 Sep-Nov;28(5-6):427-37. doi: 10.3109/08820538.2013.825288. Semin Ophthalmol. 2013. PMID: 24138051 Free PMC article. Review.
In this review, we aim to provide an update of the genetic and clinical presentation of these disorders. Disorders reviewed include Duane syndrome (DS), HOXA1 and HOXB1 syndromes, Moebius syndrome, congenital fibrosis of the extraocular muscles (CFEOM), and horizont …
In this review, we aim to provide an update of the genetic and clinical presentation of these disorders. Disorders reviewed include Duane …
Radiologic evidence for absence of the facial nerve in Mobius syndrome.
Verzijl HT, Valk J, de Vries R, Padberg GW. Verzijl HT, et al. Neurology. 2005 Mar 8;64(5):849-55. doi: 10.1212/01.WNL.0000152980.92436.D9. Neurology. 2005. PMID: 15753421
OBJECTIVE: To detail the radiologic findings in Mobius syndrome, in order to clarify its pathogenetic mechanisms. ...Radiologic findings support the notion that Mobius syndrome is part of a more complex congenital anomaly of the fossa posterior....
OBJECTIVE: To detail the radiologic findings in Mobius syndrome, in order to clarify its pathogenetic mechanisms. ...Radiologi …
38 results