HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

Histidinemia

Also Known As:
Deficiency in histidase; Histidase deficiency; Histidine ammonia-lyase deficiency
Networked: 39 relevant articles (0 outcomes, 4 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Kitagawa, Teruo: 1 article (10/2012)
2. Rojas, Denise Bertin: 1 article (05/2012)
3. Wannmacher, Clóvis Milton Duval: 1 article (05/2012)
4. de Andrade, Rodrigo Binkowski: 1 article (05/2012)
5. Gemelli, Tanise: 1 article (05/2012)
6. Campos, Aline Guimarães: 1 article (05/2012)
7. Dutra-Filho, Carlos Severo: 1 article (05/2012)
8. Zingaro, Lorenzo: 1 article (01/2005)
9. Brambilla, Maura: 1 article (01/2005)
10. Bernardi, Luigi Rossi: 1 article (01/2005)

Related Diseases

1. Maple Syrup Urine Disease
2. Galactosemias (Galactosemia)
08/01/1984 - "A follow-up study revealed the incidence of the disease in Japan: 1/108,823 for PKU; 1/450,840 for hyperphenylalaninemia (HPA); 1/1,577,939 for biopterin deficiency; 1/525,980 for MSUD; 1/1,051,959 for homocystinuria; 1/8,371 for histidinemia, and 1/788,969 for galactosemia type 1. The incidences of PKU, HPA, homocystinuria, and galactosemia (type 1) were found to be markedly low in Japan as compared with those in Caucasian countries. "
10/01/2012 - "In 1977, the Ministry of Health and Welfare (MHW) directed prefectural officials in charge of maternal and child health to start publicly funded newborn mass-screening (NBS) for phenylketonuria (PKU), maple syrup urine disease (MSUD), histidinemia, homocystinuria and galactosemia and a study group of MHW formulated the treatment guideline for the target diseases. "
08/01/1984 - "A nationwide neonatal screening program for phenylketonuria (PKU), maple syrup urine disease (MSUD), homocystinuria, histidinemia and galactosemia was started in Japan in 1977. "
01/01/1984 - "Using materials from a nationwide screening project on inborn errors of metabolism in Japan, the incidence of histidinemia, phenylketonuria, galactosemia and homocystinuria were found to be 140, 16, 14 and 7 in 1 million live births, respectively. "
01/01/2003 - "Mass newborn screening was started in October 1977 throughout Japan in order to detect five inborn errors of metabolism including phenylketonuria, maple syrup urine disease, homocystinuria, histidinemia, and galactosemia. "
3. Phenylketonurias (Phenylketonuria)
4. Homocystinuria
5. Tyrosinemias (Tyrosinemia)

Related Drugs and Biologics

1. Diamond
2. Transferases
3. Histidine Ammonia-Lyase
4. Carnitine (L-Carnitine)
5. Methylmalonic acidemia
6. Histidine (L-Histidine)
7. Adenylosuccinate lyase deficiency
8. Iminoglycinuria
9. 5'-Nucleotidase (5' Nucleotidase)
10. Serotonin (5 Hydroxytryptamine)