Jakobs C - Search Results

1

Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications.

Samson JF, Barth PG, de Vries JI, Menko FH, Ruitenbeek W, van Oost BA, Jakobs C. Samson JF, et al. Among authors: jakobs c. Eur J Pediatr. 1994 Jul;153(7):510-6. doi: 10.1007/BF01957007. Eur J Pediatr. 1994. PMID: 7957369

2

Hyperhomocysteinaemia and protein S deficiency in complicated pregnancies.

de Vries JI, Dekker GA, Huijgens PC, Jakobs C, Blomberg BM, van Geijn HP. de Vries JI, et al. Among authors: jakobs c. Br J Obstet Gynaecol. 1997 Nov;104(11):1248-54. doi: 10.1111/j.1471-0528.1997.tb10970.x. Br J Obstet Gynaecol. 1997. PMID: 9386024

3

L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenase.

Barth PG, Hoffmann GF, Jaeken J, Wanders RJ, Duran M, Jansen GA, Jakobs C, Lehnert W, Hanefeld F, Valk J, et al. Barth PG, et al. Among authors: jakobs c. J Inherit Metab Dis. 1993;16(4):753-61. doi: 10.1007/BF00711907. J Inherit Metab Dis. 1993. PMID: 8412018

4

L-2-hydroxyglutaric aciduria and lactic acidosis.

Barth PG, Wanders RJ, Scholte HR, Abeling N, Jakobs C, Schutgens RB, Vreken P. Barth PG, et al. Among authors: jakobs c. J Inherit Metab Dis. 1998 Jun;21(3):251-4. doi: 10.1023/a:1005316121584. J Inherit Metab Dis. 1998. PMID: 9686369 No abstract available.

5

Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome.

Elpeleg ON, Ruitenbeek W, Jakobs C, Barash V, De Vivo DC, Amir N. Elpeleg ON, et al. Among authors: jakobs c. J Pediatr. 1995 Jan;126(1):72-4. doi: 10.1016/s0022-3476(95)70506-6. J Pediatr. 1995. PMID: 7815230 Free article.

6

Effects of folic acid and vitamin B6 supplementation on women with hyperhomocysteinemia and a history of preeclampsia or fetal growth restriction.

Leeda M, Riyazi N, de Vries JI, Jakobs C, van Geijn HP, Dekker GA. Leeda M, et al. Among authors: jakobs c. Am J Obstet Gynecol. 1998 Jul;179(1):135-9. doi: 10.1016/s0002-9378(98)70263-7. Am J Obstet Gynecol. 1998. PMID: 9704778 Clinical Trial.

7

Underlying disorders associated with severe early-onset preeclampsia.

Dekker GA, de Vries JI, Doelitzsch PM, Huijgens PC, von Blomberg BM, Jakobs C, van Geijn HP. Dekker GA, et al. Among authors: jakobs c. Am J Obstet Gynecol. 1995 Oct;173(4):1042-8. doi: 10.1016/0002-9378(95)91324-6. Am J Obstet Gynecol. 1995. PMID: 7485291

8

Haemostatic and metabolic abnormalities in women with unexplained recurrent abortion.

Coumans AB, Huijgens PC, Jakobs C, Schats R, de Vries JI, van Pampus MG, Dekker GA. Coumans AB, et al. Among authors: jakobs c. Hum Reprod. 1999 Jan;14(1):211-4. doi: 10.1093/humrep/14.1.211. Hum Reprod. 1999. PMID: 10374122 Free article.

9

Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome.

Lopriore E, Gemke RJ, Verhoeven NM, Jakobs C, Wanders RJ, Roeleveld-Versteeg AB, Poll-The BT. Lopriore E, et al. Among authors: jakobs c. Eur J Pediatr. 2001 Feb;160(2):101-4. doi: 10.1007/s004310000644. Eur J Pediatr. 2001. PMID: 11271379 Review.

10

Infantile isolated sulphite oxidase deficiency: report of a case with negative sulphite test and normal sulphate excretion.

van der Klei-van Moorsel JM, Smit LM, Brockstedt M, Jakobs C, Dorche C, Duran M. van der Klei-van Moorsel JM, et al. Among authors: jakobs c. Eur J Pediatr. 1991 Jan;150(3):196-7. doi: 10.1007/BF01963565. Eur J Pediatr. 1991. PMID: 2044591

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