在布罗莫克里普丁治疗期间近视.

Same author

Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10.

Journal of pediatric endocrinology & metabolism : JPEM·2004

Same author

Spontaneous regression of optic gliomas: thirteen cases documented by serial neuroimaging.

Archives of ophthalmology (Chicago, Ill. : 1960)·2001

Same author

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

European journal of endocrinology·2000

Same author

Growth, puberty, and endocrine functions in patients with sporadic or familial neurofibromatosis type 1: a longitudinal study.

Pediatrics·1999

Same author

Prepubertal and pubertal growth, timing and duration of puberty and attained adult height in patients with congenital hypothyroidism (CH) detected by the neonatal screening programme for CH--a longitudinal study.

Clinical endocrinology·1998

Same author

Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height.

European journal of endocrinology·1997

相关实验视频

在布罗莫克里普丁治疗期间近视.

相关概念视频

Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10.

Spontaneous regression of optic gliomas: thirteen cases documented by serial neuroimaging.

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

Growth, puberty, and endocrine functions in patients with sporadic or familial neurofibromatosis type 1: a longitudinal study.

Prepubertal and pubertal growth, timing and duration of puberty and attained adult height in patients with congenital hypothyroidism (CH) detected by the neonatal screening programme for CH--a longitudinal study.

Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height.

相关实验视频

在布罗莫克里普丁治疗期间近视.

相关概念视频

Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10.

Spontaneous regression of optic gliomas: thirteen cases documented by serial neuroimaging.

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

Growth, puberty, and endocrine functions in patients with sporadic or familial neurofibromatosis type 1: a longitudinal study.

Prepubertal and pubertal growth, timing and duration of puberty and attained adult height in patients with congenital hypothyroidism (CH) detected by the neonatal screening programme for CH--a longitudinal study.

Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height.

相关实验视频

在布罗莫克里普丁治疗期间近视.

相关概念视频

相关文章

Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10.

Spontaneous regression of optic gliomas: thirteen cases documented by serial neuroimaging.

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

Growth, puberty, and endocrine functions in patients with sporadic or familial neurofibromatosis type 1: a longitudinal study.

Prepubertal and pubertal growth, timing and duration of puberty and attained adult height in patients with congenital hypothyroidism (CH) detected by the neonatal screening programme for CH--a longitudinal study.

Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height.

相关实验视频

在布罗莫克里普丁治疗期间近视.

相关概念视频

相关文章

Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10.

Spontaneous regression of optic gliomas: thirteen cases documented by serial neuroimaging.

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

Growth, puberty, and endocrine functions in patients with sporadic or familial neurofibromatosis type 1: a longitudinal study.

Prepubertal and pubertal growth, timing and duration of puberty and attained adult height in patients with congenital hypothyroidism (CH) detected by the neonatal screening programme for CH--a longitudinal study.

Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height.