NAV
发表于 2025-3-28 17:25:57
PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?,rhosis in PNPO deficiency. The pathogenesis is unclear but may be related to epigenetic activation of purinergic signaling in the hepatic stellate cells. PNPO deficiency may in time prove to be a suitable candidate for consideration of therapeutic orthotropic liver transplantation in select patients.
Arthropathy
发表于 2025-3-28 21:13:24
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mortgage
发表于 2025-3-29 01:00:31
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羞辱
发表于 2025-3-29 05:50:51
Pitfalls in Diagnosing Neuraminidase Deficiency: Psychosomatics and Normal Sialic Acid Excretion,ar osteonecrosis of the right femur head at age 9..Urinary oligosaccharide patterns and enzyme activity revealed neuraminidase deficiency in both patients. Urinary-bound sialic acid levels were normal. Sequencing of . demonstrated two known compound heterozygous mutations (c.1195_1200dup p.His399_Ty
有毛就脱毛
发表于 2025-3-29 10:57:44
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经典
发表于 2025-3-29 13:24:44
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痛打
发表于 2025-3-29 18:30:06
Vitamin E Improves Clinical Outcome of Patients Affected by Glycogen Storage Disease Type Ib,ount (1,583 ± 668 vs. 941 ± 809, . = 0.03) higher during vitamin E supplementation. Neutrophil function results improved during vitamin supplementation. PCDAI showed a significant reduction in the inflammatory activity during vitamin E supplementation (9 ± 1.4 vs. 13 ± 1.2, . = 0.006). In seven pati
种类
发表于 2025-3-29 23:16:34
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弯曲道理
发表于 2025-3-30 02:54:07
The Spectrum of Krabbe Disease in Greece: Biochemical and Molecular Findings,carried out in 11 unrelated cases, identified seven different mutations, four previously described (p.I250T, c.1161+6532_polyA+9kbdel, p.K139del, p.D187V) and three novel mutations (p.D610A, c.583-1 G>C, p.W132X), and seven distinct genotypes. The most prevalent mutation was mutation p.I250T, first
Capture
发表于 2025-3-30 06:59:38
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