de Coo IF - Search Results

1

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.

van der Knaap MS, Smit LM, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IF, Valk J. van der Knaap MS, et al. Among authors: de coo if. Ann Neurol. 1997 Jul;42(1):50-9. doi: 10.1002/ana.410420110. Ann Neurol. 1997. PMID: 9225685

2

Leber's hereditary optic neuropathy with the 11 778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings.

Jansen PH, van der Knaap MS, de Coo IF. Jansen PH, et al. Among authors: de coo if. J Neurol Sci. 1996 Feb;135(2):176-80. doi: 10.1016/0022-510x(95)00287-c. J Neurol Sci. 1996. PMID: 8867076

3

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome.

De Coo IF, Renier WO, Ruitenbeek W, Ter Laak HJ, Bakker M, Schägger H, Van Oost BA, Smeets HJ. De Coo IF, et al. Ann Neurol. 1999 Jan;45(1):130-3. doi: 10.1002/1531-8249(199901)45:1<130::aid-art21>3.3.co;2-q. Ann Neurol. 1999. PMID: 9894888

4

A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.

de Coo IF, Sistermans EA, de Wijs IJ, Catsman-Berrevoets C, Busch HF, Scholte HR, de Klerk JB, van Oost BA, Smeets HJ. de Coo IF, et al. Among authors: de wijs ij, de klerk jb. Neurology. 1998 Jan;50(1):293-5. doi: 10.1212/wnl.50.1.293. Neurology. 1998. PMID: 9443499

5

RYR1-related myopathies: a wide spectrum of phenotypes throughout life.

Snoeck M, van Engelen BG, Küsters B, Lammens M, Meijer R, Molenaar JP, Raaphorst J, Verschuuren-Bemelmans CC, Straathof CS, Sie LT, de Coo IF, van der Pol WL, de Visser M, Scheffer H, Treves S, Jungbluth H, Voermans NC, Kamsteeg EJ. Snoeck M, et al. Among authors: de coo if, de visser m. Eur J Neurol. 2015 Jul;22(7):1094-112. doi: 10.1111/ene.12713. Epub 2015 May 11. Eur J Neurol. 2015. PMID: 25960145

6

Clinical heterogeneity in respiratory chain complex III deficiency in childhood.

Mourmans J, Wendel U, Bentlage HA, Trijbels JM, Smeitink JA, de Coo IF, Gabreëls FJ, Sengers RC, Ruitenbeek W. Mourmans J, et al. Among authors: de coo if. J Neurol Sci. 1997 Jul;149(1):111-7. doi: 10.1016/s0022-510x(97)05379-3. J Neurol Sci. 1997. PMID: 9168175

7

A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples.

De Coo IF, Gussinklo T, Arts PJ, Van Oost BA, Smeets HJ. De Coo IF, et al. J Neurol Sci. 1997 Jul;149(1):37-40. doi: 10.1016/s0022-510x(97)05366-5. J Neurol Sci. 1997. PMID: 9168163

8

Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher disease.

Hobson GM, Davis AP, Stowell NC, Kolodny EH, Sistermans EA, de Coo IF, Funanage VL, Marks HG. Hobson GM, et al. Among authors: de coo if. Neurology. 2000 Oct 24;55(8):1089-96. doi: 10.1212/wnl.55.8.1089. Neurology. 2000. PMID: 11071483

9

Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success.

Sallevelt SC, Dreesen JC, Drüsedau M, Spierts S, Coonen E, van Tienen FH, van Golde RJ, de Coo IF, Geraedts JP, de Die-Smulders CE, Smeets HJ. Sallevelt SC, et al. Among authors: de coo if, de die smulders ce. J Med Genet. 2013 Feb;50(2):125-32. doi: 10.1136/jmedgenet-2012-101172. J Med Genet. 2013. PMID: 23339111

10

Smad1/5/8 are myogenic regulators of murine and human mesoangioblasts.

Costamagna D, Quattrocelli M, van Tienen F, Umans L, de Coo IF, Zwijsen A, Huylebroeck D, Sampaolesi M. Costamagna D, et al. Among authors: de coo if. J Mol Cell Biol. 2016 Feb;8(1):73-87. doi: 10.1093/jmcb/mjv059. Epub 2015 Oct 8. J Mol Cell Biol. 2016. PMID: 26450990 Free PMC article.

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