Results 111 to 120 of about 5,440 (220)

Primer reporte de alcaptonuria en el Perú

Revista Peruana de Medicina Experimental y Salud Pública
La alcaptonuria es un error innato del metabolismo causado por la deficiencia de la homogentisiato 1,2 dioxidasa (HGD), produciéndose un exceso de ácido homogentísico (HGA).
Daniel Guillén-Mendoza, María Quiroga de Michelena   +1 more
doaj  

Extensive Dysregulation of Phenylalanine Metabolism Is Associated With Stress Hyperphenylalaninemia and 30‐Day Death in Critically Ill Patients With Acute Decompensated Heart Failure

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Stress hyperphenylalaninemia predicts elevated mortality rates in patients with acute decompensated heart failure (ADHF). This study investigated the metabolic pathways underlying this association and identified a unique metabolic phenotype ...
Wei‐Siang Chen, Min‐Hui Liu, Yi‐Liang Tsou, Huang‐Ping Wu, Hsuan‐Ching Lin, Chung‐Yu Liang, Chao‐Hung Wang   +6 more
doaj   +1 more source

Biochemical Properties and Physiological Roles of Tyrosine Aminotransferases in Olive (Olea europaea L.)

Horticulturae
Increasing the tocopherol content in plant-derived foods not only improves their nutritional quality but may also enhance plant resilience against abiotic stress factors.
Jesús Expósito, Pilar Luaces, Rosario Sánchez, Paula Benabal, Carlos Sanz, Ana Gracia Pérez   +5 more
doaj   +1 more source

Bioaktivitas Antioksidan Biji Tumbuhan Bingkek Entada Phaseoloides Merr) [PDF]

, 2015
The use of plants as traditional medicine has long been known. One of them isBingkek (Entada phaseoloides merr). Seedl of this plant has been being used in folk medicine for stomach ache, hernias and restore the condition of women after childbirth, so as
Ade, F. Y. (Filza), Khairina, E. (Elfi), Mubarrak, J. (Jismi), Teruna, H. Y. (Hilwan)   +3 more
core  

Ochronosis ,The Rare Cause of Chronic Low Back Pain: Report of A Case

Iranian Journal of Neurosurgery, 2019
Background and Importance: Alkaptonuria is a rare genetic disorder due to deficiency of the enzyme homogentisic acid Oxidase which results in the accumulation of homogentisic acid in various body tissues; it produces a multisystemic disorder with a ...
Ali Baradaran Bagheri, Farsad Biglari, Somayeh Soroureddin, Salman Azarsina, Mohammad Kamangar   +4 more
doaj  

2-(β-d-glukopiranosiloksi) 5-hidroksi Asam Benzen Asetat Dari Biji Tumbuhan Bingkek (Entada Phaseoloides Merr) [PDF]

, 2013
Isolation of secondary metabolite compound from seeds kernel of Bingkek plant (Entada phaseoloides Merr) by column chromatographi was carried out.Extraction by maseration method with methanol, morevert the extract was partitioned using n-hexane and ethyl
Mubarrak, J. (Jismi)
core  

HOMOGENTISIC ACID OXIDASE

Journal of Biological Chemistry, 1954
Dana I. Crandall, Demetreos N. Halikis
openaire   +1 more source

Alkaptonuria: An example of a "fundamental disease"-A rare disease with important lessons for more common disorders [PDF]

, 2016
Dillon, Jane P, Gallagher, James A, Ranganath, Lakshminarayan R, Sireau, Nicolas, Timmis, Oliver   +4 more
core   +1 more source

Making rareness count: testing and pricing orphan drugs [PDF]

, 2016
This paper examines the testing and the pricing of orphan drugs, e.g. drugs for patients suffering from rare diseases. Due to the small size of these populations, orphan molecules question established evidentiary practices, namely randomized controlled ...
Doganova, Liliana, Rabeharisoa, Vololona
core   +3 more sources

CHEMICAL PREPARATION OF HOMOGENTISIC ACID

Journal of Biological Chemistry, 1949
L D, ABBOTT, J D, SMITH
openaire   +2 more sources