203 related articles for article (PubMed ID: 25803556)
41. CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
Abu-Amero KK; Bosley TM; Kondkar AA; Oystreck DT; Khan AO
Semin Ophthalmol; 2015; 30(5-6):435-42. PubMed ID: 24475916
[TBL] [Abstract][Full Text] [Related]
42. [Molecular genetic tests in advanced non-small cell lung cancer: practical relevance].
Sebastian M; Niederle N; Thomas M; Reck M; Schmittel A; Fischer B; Overbeck T; Gröschel A; Deppermann M; Pirker R; Huber RM; Eberhardt W; Griesinger F
Dtsch Med Wochenschr; 2014 Oct; 139(41):2096-100. PubMed ID: 25268213
[No Abstract] [Full Text] [Related]
43. Congenital third cranial nerve palsy with prenuclear dysinnervation involving otolithic pathways: Underpinnings of a novel congenital cranial dysinnervation disorder.
Pandey PK; Kishore D; Joon A; Saraf P
Indian J Ophthalmol; 2020 Jul; 68(7):1478-1480. PubMed ID: 32587205
[TBL] [Abstract][Full Text] [Related]
44. Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs).
Assaf AA
Eye (Lond); 2011 Oct; 25(10):1251-61. PubMed ID: 21720410
[TBL] [Abstract][Full Text] [Related]
45. Congenital fibrosis syndrome associated with central nervous system abnormalities.
Pieh C; Goebel HH; Engle EC; Gottlob I
Graefes Arch Clin Exp Ophthalmol; 2003 Jul; 241(7):546-553. PubMed ID: 12819981
[TBL] [Abstract][Full Text] [Related]
46. A Treatment Approach in Congenital Fibrosis of Extraocular Muscles.
Mravicic I; Lukacevic S; Biscevic A; Pjano MA; Ziga N; Tusek M
Med Arch; 2023 Apr; 77(2):137-141. PubMed ID: 37260807
[TBL] [Abstract][Full Text] [Related]
47. Oculomotility disorders arising from disruptions in brainstem motor neuron development.
Engle EC
Arch Neurol; 2007 May; 64(5):633-7. PubMed ID: 17502461
[TBL] [Abstract][Full Text] [Related]
48. MRI evaluation of cranial nerve abnormalities and extraocular muscle fibrosis in duane retraction syndrome and congenital extraocular muscle fibrosis.
Yang T; Li X; Wang K; Zhang Q; Hao R; Zhang W
Graefes Arch Clin Exp Ophthalmol; 2024 Mar; ():. PubMed ID: 38530452
[TBL] [Abstract][Full Text] [Related]
49. CFEOM3: a new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3.
Doherty EJ; Macy ME; Wang SM; Dykeman CP; Melanson MT; Engle EC
Invest Ophthalmol Vis Sci; 1999 Jul; 40(8):1687-94. PubMed ID: 10393037
[TBL] [Abstract][Full Text] [Related]
50. Congenital Fibrosis of the Extraocular Muscles: An Overview from Genetics to Management.
Xia W; Wei Y; Wu L; Zhao C
Children (Basel); 2022 Oct; 9(11):. PubMed ID: 36360333
[TBL] [Abstract][Full Text] [Related]
51. Splitting of the extraocular horizontal rectus muscle in congenital cranial dysinnervation disorders.
Okanobu H; Kono R; Miyake K; Ohtsuki H
Am J Ophthalmol; 2009 Mar; 147(3):550-556.e1. PubMed ID: 19038376
[TBL] [Abstract][Full Text] [Related]
52. Congenital fibrosis of the extraocular muscles (CFEOM) syndrome associated with progressive cerebellar ataxia.
Yoshida K; Okano T; Hoshi K; Yahikozawa H; Suzuki K; Banno H; Tamura T; Sobue G; Ikeda S
Am J Med Genet A; 2007 Jul; 143A(13):1494-501. PubMed ID: 17551929
[TBL] [Abstract][Full Text] [Related]
53. [Inherited ophthalmological disorders. Part 1: Genetic fundamentals and phenotypes].
Preising MN; Stieger K; Lorenz B
Klin Monbl Augenheilkd; 2014 Feb; 231(2):177-89; quiz 190-1. PubMed ID: 24532407
[No Abstract] [Full Text] [Related]
54. Congenital Ptosis Associated With Adduction as a Dysinnervation Disorder: A Report of a Rare Case.
Alnosair G; Alhashim H; Alhamoud M; Alturki H
Cureus; 2023 Jun; 15(6):e40422. PubMed ID: 37456445
[TBL] [Abstract][Full Text] [Related]
55. [Genetic diseases of the eye].
Besch D; Rudolph G
Klin Monbl Augenheilkd; 2005 Dec; 222(12):955-71. PubMed ID: 16380882
[TBL] [Abstract][Full Text] [Related]
56. Possible association of congenital Brown syndrome with congenital cranial dysinnervation disorders.
Ellis FJ; Jeffery AR; Seidman DJ; Sprague JB; Coussens T; Schuller J
J AAPOS; 2012 Dec; 16(6):558-64. PubMed ID: 23237754
[TBL] [Abstract][Full Text] [Related]
57. A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome.
Ali Z; Xing C; Anwar D; Itani K; Weakley D; Gong X; Pascual JM; Mootha VV
Mol Vis; 2014; 20():368-75. PubMed ID: 24715754
[TBL] [Abstract][Full Text] [Related]
58. Genetics of inherited platelet disorders.
Gothwal M; Sandrock-Lang K; Zieger B
Hamostaseologie; 2014; 34(2):133-41. PubMed ID: 24352347
[TBL] [Abstract][Full Text] [Related]
59. Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles.
Engle EC; Goumnerov BC; McKeown CA; Schatz M; Johns DR; Porter JD; Beggs AH
Ann Neurol; 1997 Mar; 41(3):314-25. PubMed ID: 9066352
[TBL] [Abstract][Full Text] [Related]
60. [Hereditary ectopia lentis].
Neuhann TM
Klin Monbl Augenheilkd; 2015 Mar; 232(3):259-65. PubMed ID: 25654236
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]