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5. Peroxisomal disorder-unusual presentation as failure to thrive in early infancy. Kalyanasundaram S; Ibhanesebhor SE; Manjunatha CM Indian J Pediatr; 2010 Oct; 77(10):1151-2. PubMed ID: 20872098 [TBL] [Abstract][Full Text] [Related]
6. Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency. Sorlin A; Briand G; Cheillan D; Wiedemann A; Montaut-Verient B; Schmitt E; Feillet F Neuropediatrics; 2016 Jun; 47(3):179-81. PubMed ID: 26947510 [TBL] [Abstract][Full Text] [Related]
7. Pigmentary retinopathy of myotonic dystrophy. Betten MG; Bilchik RC; Smith ME Am J Ophthalmol; 1971 Oct; 72(4):720-3. PubMed ID: 5110863 [No Abstract] [Full Text] [Related]
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13. The clinical presentation of mitochondrial diseases in children with progressive intellectual and neurological deterioration: a national, prospective, population-based study. Verity CM; Winstone AM; Stellitano L; Krishnakumar D; Will R; McFarland R Dev Med Child Neurol; 2010 May; 52(5):434-40. PubMed ID: 19747204 [TBL] [Abstract][Full Text] [Related]
14. [The importance of semiology and biochemistry in the diagnostic management of a peroxisomal biogenesis disorder]. Cote-Orozco JE; Echeverri-Pena OY; Guevara-Morales JM; Espinosa E Rev Neurol; 2018 Oct; 67(8):298-302. PubMed ID: 30289153 [TBL] [Abstract][Full Text] [Related]
19. The peroxisome and the eye. Folz SJ; Trobe JD Surv Ophthalmol; 1991; 35(5):353-68. PubMed ID: 1710072 [TBL] [Abstract][Full Text] [Related]
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