Cochrane Database Syst Rev
Drug treatment for spinal muscular atrophy types II and III.
Wadman RI, van der Pol WL, Bosboom WM, Asselman FL, van den Berg LH, Iannaccone ST, Vrancken AF
Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or a heterozygous deletio ...
Read More
Source: PubMed
Maturitas
Psychological behavior patterns and coping with menopausal symptoms among users and non-users of hormone replacement therapy in Finnish cohorts of women aged 52-56 years.
Jalava-Broman J, Junttila N, Sillanmäki L, Mäkinen J, Rautava P
To identify subgroups of women who differ with respect to self-evaluated stress, hostility, optimism and sense of coherence, and to identify differenc ...
Read More
Source: PubMed
Gynecol Obstet Fertil Senol 2020 Jan 28
[Borderline ovarian tumours: CNGOF Guidelines for clinical practice - Epidemiological aspects and risk factors].
Ouldamer L, Body G, Daraï E, Bendifallah S
The incidence (rate /100,000) of BOT gradually increases with age from 15-19 years of age and peaks at nearly 4.5 cases/100,000 for the 55-59 year age ...
Read More
Source: PubMed
Front Pediatr
Congenital Isolated ACTH Deficiency Caused by TBX19 Gene Mutation: A Family Report.
Peng C, Sun G, Tang Z, Hou X
Congenital isolated adrenocorticotropic hormone deficiency (CIAD) is a rare disorder that may be conducive to hypoglycemia, cholestasis, and seizures. ...
Read More
Source: PubMed
Front Endocrinol (Lausanne)
Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System.
Ueda K, Adachi Y, Liu P, Fukuma N, Takimoto E
Premenopausal females have a lower incidence of death from cardiovascular disease (CVD) than male counterparts, supporting the notion that estrogen is ...
Read More
Source: PubMed
Cochrane Database Syst Rev
Drug treatment for spinal muscular atrophy types II and III.
Wadman RI, van der Pol WL, Bosboom WM, Asselman FL, van den Berg LH, Iannaccone ST, Vrancken AF
Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or a heterozygous deletio ...
Read More
Source: PubMed
Maturitas
Psychological behavior patterns and coping with menopausal symptoms among users and non-users of hormone replacement therapy in Finnish cohorts of women aged 52-56 years.
Jalava-Broman J, Junttila N, Sillanmäki L, Mäkinen J, Rautava P
To identify subgroups of women who differ with respect to self-evaluated stress, hostility, optimism and sense of coherence, and to identify differenc ...
Read More
Source: PubMed
Gynecol Obstet Fertil Senol 2020 Jan 28
[Borderline ovarian tumours: CNGOF Guidelines for clinical practice - Epidemiological aspects and risk factors].
Ouldamer L, Body G, Daraï E, Bendifallah S
The incidence (rate /100,000) of BOT gradually increases with age from 15-19 years of age and peaks at nearly 4.5 cases/100,000 for the 55-59 year age ...
Read More
Source: PubMed
Front Pediatr
Congenital Isolated ACTH Deficiency Caused by TBX19 Gene Mutation: A Family Report.
Peng C, Sun G, Tang Z, Hou X
Congenital isolated adrenocorticotropic hormone deficiency (CIAD) is a rare disorder that may be conducive to hypoglycemia, cholestasis, and seizures. ...
Read More
Source: PubMed
Front Endocrinol (Lausanne)
Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System.
Ueda K, Adachi Y, Liu P, Fukuma N, Takimoto E
Premenopausal females have a lower incidence of death from cardiovascular disease (CVD) than male counterparts, supporting the notion that estrogen is ...
Read More
Source: PubMed
Cochrane Database Syst Rev
Drug treatment for spinal muscular atrophy types II and III.
Wadman RI, van der Pol WL, Bosboom WM, Asselman FL, van den Berg LH, Iannaccone ST, Vrancken AF
Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or a heterozygous deletio ...
Read More
Source: PubMed
Maturitas
Psychological behavior patterns and coping with menopausal symptoms among users and non-users of hormone replacement therapy in Finnish cohorts of women aged 52-56 years.
Jalava-Broman J, Junttila N, Sillanmäki L, Mäkinen J, Rautava P
To identify subgroups of women who differ with respect to self-evaluated stress, hostility, optimism and sense of coherence, and to identify differenc ...
Read More
Source: PubMed
Gynecol Obstet Fertil Senol 2020 Jan 28
[Borderline ovarian tumours: CNGOF Guidelines for clinical practice - Epidemiological aspects and risk factors].
Ouldamer L, Body G, Daraï E, Bendifallah S
The incidence (rate /100,000) of BOT gradually increases with age from 15-19 years of age and peaks at nearly 4.5 cases/100,000 for the 55-59 year age ...
Read More
Source: PubMed
Front Pediatr
Congenital Isolated ACTH Deficiency Caused by TBX19 Gene Mutation: A Family Report.
Peng C, Sun G, Tang Z, Hou X
Congenital isolated adrenocorticotropic hormone deficiency (CIAD) is a rare disorder that may be conducive to hypoglycemia, cholestasis, and seizures. ...
Read More
Source: PubMed
Front Endocrinol (Lausanne)
Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System.
Ueda K, Adachi Y, Liu P, Fukuma N, Takimoto E
Premenopausal females have a lower incidence of death from cardiovascular disease (CVD) than male counterparts, supporting the notion that estrogen is ...
Read More
Source: PubMed
