Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yue-Cheng Lu"'
Publikováno v:
Journal of Obstetrics and Gynaecology. 39:275-277
The 49,XXXXY syndrome is a rare chromosomal aneuploidy. It used to be labelled as a ‘Klinefelter variant’, but differs from the latter in many ways and is more severe (Tartaglia et al. 2011). The s...
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 211:225-227
Publikováno v:
Hemoglobin. 41:47-49
We first report a novel β chain variant, Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G], in a Chinese family. Heterozygous inheritance of the mutation results in a mild β-thalassemia (β-thal) phenotype, whereas compound heterozygosity of Hb Heze wit
Publikováno v:
BioMed Research International
Diabetic neuropathy pain (DNP), a spontaneous pain with hyperalgesia and allodynia, greatly compromises patients' quality of life. Our previous study suggested that dexmedetomidine (DEX) can relieve hyperalgesia in rats by inhibiting inflammation and
Publikováno v:
BioMed Research International, Vol 2018 (2018)
Diabetic neuropathy pain (DNP), a spontaneous pain with hyperalgesia and allodynia, greatly compromises patients’ quality of life. Our previous study suggested that dexmedetomidine (DEX) can relieve hyperalgesia in rats by inhibiting inflammation a
First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok
Publikováno v:
Hemoglobin. 40:425-427
The double heterozygosity for α and β chain variants leads to the formation of abnormal heterodimer hybrids, which could render laboratory diagnostics in a routine setting difficult. The following is the first report of a double heterozygosity for