Results 91 to 100 of about 32,896 (166)

Wilson's disease: A patient undiagnosed for 18 years [PDF]

, 2006
Wilson's disease, an autosomal recessive disorder of copper metabolism, is the most common inherited hepatic disease in Hong Kong. Diagnosis is based on the presence of Kayser-Fleischer rings, typical neurological symptoms, and/or a low serum ...
Fan, ST, Lam, CW, Liu, CL, Mak, CM, Tam, S   +4 more
core  

Keragaman Protein Plasma Darah Kambing Jawarandu di Kabupaten Pemalang [PDF]

, 2013
The aim of this study was to evaluate the variability of blood proteins plasma from Jawarandu goat at six loci by simultaneously. A total of 24 samples of blood protein plasm of Jawarandu goat from Pemalang District was taken.
Brata, G. D. (Galih), Kurnianto, E. (Edy), Sutopo, S. (Sutopo)   +2 more
core  

Acute phase proteins in tuberculous patients [PDF]

, 1990
The serum concentrations of some acute phase proteins were determined on admission, during treatment, at the end of treatment and at 12 months after stopping treatment in 20 patients with pulmonary tuberculosis.
Acharyulu, G S, Immanuel, Chandra, Kannapiran, M, Raghupati Sarma, G, Segaran, R   +4 more
core  

TDMQ20 as A Drug Candidate for Wilson’s Disease: Comparison with D-Penicillamine, Trientine, and Tetrathiomolybdate In Vitro and In Mice

Pharmaceutics
Background/Objectives: The lifelong treatment of Wilson’s disease (WD) currently relies on copper chelators with relatively poor metal specificity, which frequently exhibit serious adverse effects.
Yingshan Zhu, Weiling Peng, Guangwei Liu, Longxin Li, Zikang Zhou, Michel Nguyen, Anne Robert, Yan Liu, Bernard Meunier   +8 more
doaj   +1 more source

Impact of Parenteral Copper and Zinc Administration on Reproduction, Inflammation, and Antioxidant Responses of Bos indicus Beef Heifers

Animals
Two experiments evaluated the effects of copper (Cu) and zinc (Zn) injection on body weight (BW), body condition score (BCS), pregnancy rate, ovarian traits, and antioxidant and inflammatory responses of beef heifers. In Exp.
Luana Gomes da Silva, Marcelo Vedovatto, Juliana Ranches, Edilane Costa Martins, Matheus Fellipe Ferreira, Eduardo de Assis Lima, Luiz Carlos Louzada Ferreira, Willian Vaniel Alves dos Reis, Gumercindo Loriano Franco   +8 more
doaj   +1 more source

Adult‐Onset Acute Cerebellar Ataxia with Preceding Essential Tremor‐like Syndrome Associated with a Novel Variant in ATP1A3

Movement Disorders Clinical Practice, Volume 13, Issue 3, Page 832-834, March 2026.
Lukas Gattermeyer‐Kell, Sebastian Franthal, Maria Tscherner, Mariella Kögl, Petra Katschnig‐Winter, Christian Windpassinger, Petra Schwingenschuh   +6 more
wiley   +1 more source

Differential Regulation of Ceruloplasmin Isoforms Expression in Macrophages and Hepatocytes [PDF]

, 2011
Prémio de melhor poster.Ceruloplasmin (Cp) is an acute-phase protein that has been implicated in iron metabolism due to its ferroxidase activity, assisting ferroportin (Fpn) on cellular iron efflux.
Auriac, A., Banha, J., Canonne-Hergaux, F., Costa, L., Marques, L., Silva, B., Willemetz, A.   +6 more
core  

Molecular and pathological basis of aceruloplasminemia

Biological Research, 2006
Aceruloplasminemia is an autosomal recessive neurodegenerative disease characterized by iron accumulation in the brain as well as visceral organs. It is a loss-of-function disorder caused by mutations in the ceruloplasmin gene.
SATOSHI KONO, HIROAKI MIYAJIMA
doaj  

Exploring the interplay of prolactin and bromocriptine on serum markers in granulomatous lobular mastitis

Frontiers in Immunology
ObjectiveIn this study, we retrospectively analyzed the relationship between PRL level and serum inflammatory and immune markers in patients with granulomatous lobular mastitis (GLM) and analyzed the effect of bromocriptine treatment on serum ...
Binheng Liu, Wenchao Qu, Yi Feng, Xueqing Wu, Jiamei Feng, Qingqian Gao, Shijun Shao, Jiaye Sun, Hua Wan, Weiping Chen   +9 more
doaj   +1 more source

Lafora Disease Masquerading as Hepatic Dysfunction [PDF]

, 2018
Lafora disease is fatal intractable progressive myoclonic epilepsy. It is frequently characterized by epileptic seizures, difficulty walking, muscle spasms, and dementia in late childhood or adolescence.
Abdullah, Hafez Mohammad A., Ali, Nouman Safdar, Ilyas, Ghulam, Inayat, Faisal, Khan, Zarak H., Lodhi, Hanan T., Ullah, Waqas   +6 more
core   +1 more source