|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
Hormonal background of the hypertension and fluid derangements associated with adrenocorticotrophic hormone treatment of infants.
|
2551692 |
1989 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Cardiac vagal activation by adrenocorticotropic hormone treatment in infants with West syndrome.
|
17287597 |
2007 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
Thiazide therapy for ACTH-induced hypercalciuria and nephrolithiasis.
|
1324751 |
1992 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
Hypertrophic cardiomyopathy during corticotropin therapy for infantile spasms. A clinical and echocardiographic study.
|
8381257 |
1993 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Decreased cerebrospinal fluid levels of beta-endorphin and ACTH in children with infantile spasms.
|
11341487 |
2001 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
[Treatment of infantile spasms with long-term low dose ACTH].
|
1327015 |
1992 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Adrenocorticotropic hormone and vigabatrin treatment of children with infantile spasms underlying cerebral palsy.
|
8980841 |
1997 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
ACTH therapy in infantile spasms: side effects.
|
6254450 |
1980 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Induced microseizures in West syndrome.
|
1656808 |
1991 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
[Lethal side effects from ACTH-therapy in infantile spasm (author's transl)].
|
6107850 |
1980 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Clinical profile and treatment of infantile spasms using vigabatrin and ACTH--a developing country perspective.
|
20078871 |
2010 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
[Secondary myocardial hypertrophy in newborn infants and infants without congenital heart defect].
|
2853496 |
1988 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
[Treatment of infantile spasms with long-term low dose ACTH].
|
1327015 |
1992 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
Decreased cerebrospinal fluid levels of beta-endorphin and ACTH in children with infantile spasms.
|
11341487 |
2001 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
Induced microseizures in West syndrome.
|
1656808 |
1991 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
[Hypertrophic myocardiopathy during the corticotropin treatment of infantile spasms].
|
8928979 |
1996 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
disease |
CTD_human |
ACTH-induced seizures in an infant with West syndrome.
|
2554740 |
1989 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
[How effective is the treatment schedule in children with infantile spasms?].
|
2983143 |
1985 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
disease |
CTD_human |
[Lethal side effects from ACTH-therapy in infantile spasm (author's transl)].
|
6107850 |
1980 |
|
| Entrez Id: |
7248 |
| Gene Symbol: |
TSC1 |
TSC1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Management of epilepsy in tuberous sclerosis complex.
|
18345974 |
2008 |
|
| Entrez Id: |
7249 |
| Gene Symbol: |
TSC2 |
TSC2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Management of epilepsy in tuberous sclerosis complex.
|
18345974 |
2008 |
|
| Entrez Id: |
51733 |
| Gene Symbol: |
UPB1 |
UPB1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Five cases of beta-ureidopropionase deficiency detected by GC/MS analysis of urine metabolome.
|
18853477 |
2009 |