ライフサイエンスコーパス: congenital hypothyroidism

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1 tial therapeutic targets in the treatment of congenital hypothyroidism.

2 UOX expression and the molecular genetics of congenital hypothyroidism.

3 ons may induce constitutive inactivation and congenital hypothyroidism.

4 e sequencing data in patients suffering from congenital hypothyroidism.

5 humans is associated with the development of congenital hypothyroidism.

6 diabetes mellitus and psoriasis, and 1 with congenital hypothyroidism and nephrotic syndrome.

7 in differentiating transient from permanent congenital hypothyroidism and predicting the response of

8 Congenital hypothyroidism and the thyroid hormone (T(3))

9 In a number of human kindreds suffering from congenital hypothyroidism, and in the cog congenital goi

10 plicated in glucose/galactose malabsorption, congenital hypothyroidism, Bartter's syndrome, epilepsy,

11 Overview of congenital hypothyroidism caused by thyroid hormone synt

12 Central congenital hypothyroidism (CCH) is more prevalent in chi

13 t result in a non-functional protein lead to congenital hypothyroidism due to I(-) transport defect (

14 Congenital hypothyroidism due to thyroid dyshormonogenes

15 The introduction of screening for congenital hypothyroidism has led to a marked improvemen

16 These results suggest that congenital hypothyroidism impairs learning when a discri

17 have linked mutations in the ChEL domain to congenital hypothyroidism in humans and rodents; these m

18 Mutations in DUOX2 produce congenital hypothyroidism in humans.

19 tosomal recessive trait, deficient Tg causes congenital hypothyroidism in newborns that, if untreated

20 The Tg-G2320R mutation is responsible for congenital hypothyroidism in rdw/rdw rats, in which a la

21 fully rescue the high mortality rate due to congenital hypothyroidism in these mice.

22 Morphologic alterations associated with congenital hypothyroidism include the absence of detecta

23 20R (G221R in NLGN) mutation responsible for congenital hypothyroidism into NLGN3, we show that mutat

24 Congenital hypothyroidism is the most common neonatal en

25 cause the syndrome of neonatal diabetes and congenital hypothyroidism (NDH).

26 Congenital hypothyroidism occurs in one of every three t

27 Primary congenital hypothyroidism (PCH) is currently detected ef

28 roglobulin can result in autosomal recessive congenital hypothyroidism with deficient thyroglobulin.

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