Van Goethem G - Search Results

1

Serum erythropoietin levels in elderly inpatients with anemia of chronic disorders and iron deficiency anemia.

Joosten E, Van Hove L, Lesaffre E, Goossens W, Dereymaeker L, Van Goethem G, Pelemans W. Joosten E, et al. Among authors: van goethem g, van hove l. J Am Geriatr Soc. 1993 Dec;41(12):1301-4. doi: 10.1111/j.1532-5415.1993.tb06479.x. J Am Geriatr Soc. 1993. PMID: 8227911

2

Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism.

Devriendt K, Keymolen K, Roelen L, Van Goethem G, Meireleire J, Fryns JP. Devriendt K, et al. Among authors: van goethem g. Clin Dysmorphol. 2000 Apr;9(2):111-4. doi: 10.1097/00019605-200009020-00007. Clin Dysmorphol. 2000. PMID: 10826622

3

Fatal encephalitis caused by Mycoplasma pneumoniae diagnosed by the polymerase chain reaction.

Ieven M, Demey H, Ursi D, Van Goethem G, Cras P, Goossens H. Ieven M, et al. Among authors: van goethem g. Clin Infect Dis. 1998 Dec;27(6):1552-3. doi: 10.1086/517753. Clin Infect Dis. 1998. PMID: 9868691 No abstract available.

4

Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1q.

Lukusa T, Van Buggenhout G, Devriendt K, Meireleire J, Van Goethem G, Roelen L, Fryns JP. Lukusa T, et al. Among authors: van goethem g, van buggenhout g. Ann Genet. 1998;41(4):199-204. Ann Genet. 1998. PMID: 9881182 Review.

5

Novel syndromic form of X-linked complicated spastic paraplegia.

Claes S, Devriendt K, Van Goethem G, Roelen L, Meireleire J, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Among authors: van goethem g. Am J Med Genet. 2000 Sep 4;94(1):1-4. doi: 10.1002/1096-8628(20000904)94:1<1::aid-ajmg1>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10982473

6

3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability.

Vergaelen E, Swillen A, Van Esch H, Claes S, Van Goethem G, Devriendt K. Vergaelen E, et al. Among authors: van goethem g. Eur J Med Genet. 2015 Apr;58(4):244-8. doi: 10.1016/j.ejmg.2015.01.008. Epub 2015 Feb 3. Eur J Med Genet. 2015. PMID: 25655469

7

Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern.

Fieremans N, Van Esch H, Holvoet M, Van Goethem G, Devriendt K, Rosello M, Mayo S, Martinez F, Jhangiani S, Muzny DM, Gibbs RA, Lupski JR, Vermeesch JR, Marynen P, Froyen G. Fieremans N, et al. Among authors: van goethem g. Hum Mutat. 2016 Aug;37(8):804-11. doi: 10.1002/humu.23012. Epub 2016 May 25. Hum Mutat. 2016. PMID: 27159028 Free PMC article.

8

Spectrum of Movement Disorders in 18p Deletion Syndrome.

Crosiers D, Blaumeiser B, Van Goethem G. Crosiers D, et al. Among authors: van goethem g. Mov Disord Clin Pract. 2018 Dec 6;6(1):70-73. doi: 10.1002/mdc3.12707. eCollection 2019 Jan. Mov Disord Clin Pract. 2018. PMID: 30746419 Free PMC article.

9

Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.

Rooms L, Reyniers E, Wuyts W, Storm K, van Luijk R, Scheers S, Wauters J, van den Ende J, Biervliet M, Eyskens F, van Goethem G, Laridon A, Ceulemans B, Courtens W, Kooy RF. Rooms L, et al. Among authors: van goethem g, van luijk r, van den ende j. Clin Genet. 2006 Jan;69(1):58-64. doi: 10.1111/j.1399-0004.2005.00545.x. Clin Genet. 2006. PMID: 16451137

10

Patient homozygous for a recessive POLG mutation presents with features of MERRF.

Van Goethem G, Mercelis R, Löfgren A, Seneca S, Ceuterick C, Martin JJ, Van Broeckhoven C. Van Goethem G, et al. Among authors: van broeckhoven c. Neurology. 2003 Dec 23;61(12):1811-3. doi: 10.1212/01.wnl.0000098997.23471.65. Neurology. 2003. PMID: 14694057

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