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Items: 4

1.

Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11.

Reinson K, Kovacs-Nagy R, Õiglane-Shlik E, Pajusalu S, Nõukas M, Wintjes LT, van den Brandt FCA, Brink M, Acker T, Ahting U, Hahn A, Schänzer A, Haack TB, Rodenburg RJ, Õunap K.

Eur J Med Genet. 2018 Nov 10:103572. doi: 10.1016/j.ejmg.2018.11.006. [Epub ahead of print]

PMID:
30423443
2.

A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy.

Jonckheere AI, Hogeveen M, Nijtmans LG, van den Brand MA, Janssen AJ, Diepstra JH, van den Brandt FC, van den Heuvel LP, Hol FA, Hofste TG, Kapusta L, Dillmann U, Shamdeen MG, Smeitink JA, Rodenburg RJ.

J Med Genet. 2008 Mar;45(3):129-33. Epub 2007 Oct 22.

PMID:
17954552
3.

Measurement of peritoneal fluid handling in children on continuous ambulatory peritoneal dialysis using autologous hemoglobin.

Reddingius RE, Schröder CH, Willems HL, van den Brandt FC, Koomen GC, Krediet RT, Monnens LA.

Perit Dial Int. 1994;14(1):42-7.

PMID:
8312413
4.

Familial selective IgA deficiency with circulating anti-IgA antibodies: a distinct group of patients?

de Laat PC, Weemaes CM, Bakkeren JA, van den Brandt FC, van Lith TG, de Graaf R, van Munster PJ, Stoelinga GB.

Clin Immunol Immunopathol. 1991 Jan;58(1):92-101.

PMID:
1983972

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