140 related articles for article (PubMed ID: 8688100)
1. Fetal polycystic kidney disease associated with glutaric aciduria type II: an inborn error of energy metabolism.
Whitfield J; Hurst D; Bennett MJ; Sherwood WG; Hogg R; Gonsoulin W
Am J Perinatol; 1996 Apr; 13(3):131-4. PubMed ID: 8688100
[TBL] [Abstract][Full Text] [Related]
2. Glutaric aciduria type II, an unusual cause of prenatal polycystic kidneys: report of prenatal diagnosis and confirmation of autosomal recessive inheritance.
Hockey A; Knowles S; Davies D; Carey W; Hurst J; Goldblatt J
Birth Defects Orig Artic Ser; 1993; 29(1):373-82. PubMed ID: 8280889
[No Abstract] [Full Text] [Related]
3. Recurrent fetal polycystic kidneys associated with glutaric aciduria type II.
Kjaergaard S; Graem N; Larsen T; Skovby F
APMIS; 1998 Dec; 106(12):1188-93. PubMed ID: 10052728
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes.
Chisholm CA; Vavelidis F; Lovell MA; Sweetman L; Roe CR; Roe DS; Frerman FE; Wilson WG
Prenat Diagn; 2001 Oct; 21(10):856-9. PubMed ID: 11746129
[TBL] [Abstract][Full Text] [Related]
5. Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities.
Hackl A; Mehler K; Gottschalk I; Vierzig A; Eydam M; Hauke J; Beck BB; Liebau MC; Ensenauer R; Weber LT; Habbig S
Pediatr Nephrol; 2017 May; 32(5):791-800. PubMed ID: 28083701
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of autosomal recessive polycystic kidney disease: variable outcome within one family.
Barth RA; Guillot AP; Capeless EL; Clemmons JJ
Am J Obstet Gynecol; 1992 Feb; 166(2):560-1. PubMed ID: 1536230
[TBL] [Abstract][Full Text] [Related]
7. [Atypical course of a multiple acyl-CoA-dehydrogenase deficiency].
Rose M; Matern D; Millington DS; Lehnert W
Klin Padiatr; 1999; 211(5):413-6. PubMed ID: 10572901
[TBL] [Abstract][Full Text] [Related]
8. Antenatal expression of multiple acyl-CoA dehydrogenase deficiency.
Vianey-Saban C; Bouvier R; Cochat P; Buenerd A; Divry P; Dumoulin R; Cordier MP
J Inherit Metab Dis; 2000 Jun; 23(4):345-8. PubMed ID: 10896290
[No Abstract] [Full Text] [Related]
9. Postnatal and antenatal laboratory diagnosis of glutaric aciduria II in a South African family.
Henderson HE; Balla R; de Jong G; Piek CJ; Mienie LJ; Erasmus E
S Afr Med J; 1987 May; 71(9):589-91. PubMed ID: 3576410
[TBL] [Abstract][Full Text] [Related]
10. Prenatal cerebral ultrasound and MRI findings in glutaric aciduria Type 1: a de novo case.
Mellerio C; Marignier S; Roth P; Gaucherand P; des Portes V; Pracros JP; Guibaud L
Ultrasound Obstet Gynecol; 2008 Jun; 31(6):712-4. PubMed ID: 18470866
[No Abstract] [Full Text] [Related]
11. Multiple acyl-CoA-dehydrogenase deficiency (MADD): use of acylcarnitines and fatty acids to monitor the response to dietary treatment.
Abdenur JE; Chamoles NA; Schenone AB; Jorge L; Guinle A; Bernard C; Levandovskiy V; Fusta M; Lavorgna S
Pediatr Res; 2001 Jul; 50(1):61-6. PubMed ID: 11420420
[TBL] [Abstract][Full Text] [Related]
12. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.
Lehnert W; Wendel U; Lindenmaier S; Böhm N
Eur J Pediatr; 1982 Sep; 139(1):56-9. PubMed ID: 7173259
[No Abstract] [Full Text] [Related]
13. Prenatal diagnosis of autosomal recessive polycystic kidney disease. A case report.
Mine K; Suzuki S; Watanabe S; Sawa R; Yoneyama Y; Asakura H; Araki T
Nihon Ika Daigaku Zasshi; 1999 Jun; 66(3):188-90. PubMed ID: 10401236
[TBL] [Abstract][Full Text] [Related]
14. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.
Böhm N; Uy J; Kiessling M; Lehnert W
Eur J Pediatr; 1982 Sep; 139(1):60-5. PubMed ID: 7173260
[No Abstract] [Full Text] [Related]
15. Compliance to clinical guidelines determines outcome in glutaric aciduria type I in the era of newborn screening.
Höliner I; Simma B; Reiter A; Sass JO; Zschocke J; Huemer M
Klin Padiatr; 2010; 222(1):35-7. PubMed ID: 20084589
[TBL] [Abstract][Full Text] [Related]
16. [Prenatal diagnosis and clinical prognosis of fetal hyperechogenic kidneys].
Li H; Liu T; Liu C; Shang T
Zhonghua Fu Chan Ke Za Zhi; 2007 Apr; 42(4):236-8. PubMed ID: 17631762
[TBL] [Abstract][Full Text] [Related]
17. Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation.
Khurana S; Saini V; Wadhwa V; Kaur H
J Ultrasound; 2017 Jun; 20(2):167-170. PubMed ID: 28593008
[TBL] [Abstract][Full Text] [Related]
18. Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency.
Morris AA; Olpin SE; Van't Hoff WG; Johnson AW; Leonard JV
J Inherit Metab Dis; 1997 Aug; 20(4):604-5. PubMed ID: 9266400
[No Abstract] [Full Text] [Related]
19. [Echographic screening for autosomal dominant polycystic kidney disease from intrauterine life to adult life].
Serbelloni P; Conte F; Garavaglia G; Spattini A; Sessa A
Arch Ital Urol Nefrol Androl; 1991 Jun; 63 Suppl 2():89-92. PubMed ID: 1836669
[TBL] [Abstract][Full Text] [Related]
20. Magnetic resonance imaging findings of adult-onset glutaric aciduria type I.
Sonmez G; Mutlu H; Ozturk E; Sildiroglu HO; Keskin AT; Basekim CC; Kizilkaya E
Acta Radiol; 2007 Jun; 48(5):557-9. PubMed ID: 17520433
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]