Use of hematin in tyrosinemia type I

被引:0
作者
Williams, Monika [1 ]
Hildebrandt, Clara [1 ]
机构
[1] Univ N Carolina, Div Pediat Genet & Metab, Dept Pediat, Chapel Hill, NC 27515 USA
关键词
D O I
10.1016/j.ymgme.2024.108272
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Poster # 0
引用
收藏
页数:1
相关论文
共 50 条
[21]   Neurological and Neuropsychological Problems in Tyrosinemia Type I Patients [J].
van Ginkel, Willem G. ;
Jahja, Rianne ;
Huijbregts, Stephan C. J. ;
van Spronsen, Francjan J. .
HEREDITARY TYROSINEMIA: PATHOGENESIS, SCREENING AND MANAGEMENT, 2017, 959 :111-122
[22]   LABORATORY MONITORING OF PATIENTS WITH HEREDITARY TYROSINEMIA TYPE I [J].
Schultz, Matthew ;
Netzel, Brian ;
Singh, Rani ;
Gavrilov, Dimitar ;
Oglesbee, Devin ;
Raymond, Kimiyo ;
Rinaldo, Piero ;
Tortorelli, Silvia ;
Matern, Dietrich .
MOLECULAR GENETICS AND METABOLISM, 2019, 126 (03) :324-325
[23]   VISCERAL PATHOLOGY OF HEREDITARY TYROSINEMIA TYPE-I [J].
RUSSO, P ;
OREGAN, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 47 (02) :317-324
[24]   Tyrosinemia type I - Diagnostic issues and prenatal diagnosis [J].
Bijarnia S. ;
Puri R.D. ;
Ruel J. ;
Gray G.F. ;
Jenkinson L. ;
Verma I.C. .
The Indian Journal of Pediatrics, 2006, 73 (2) :163-165
[25]   Tyrosinemia Type I in Japan: A Report of Five Cases [J].
Nakamura, Kimitoshi ;
Ito, Michinori ;
Shigematsu, Yosuke ;
Endo, Fumio .
HEREDITARY TYROSINEMIA: PATHOGENESIS, SCREENING AND MANAGEMENT, 2017, 959 :133-138
[26]   LABORATORY MONITORING OF PATIENTS WITH HEREDITARY TYROSINEMIA TYPE I [J].
Schultz, Matthew ;
Netzel, Brian ;
Singh, Rani ;
Gavrilov, Dimitar ;
Oglesbee, Devin ;
Raymond, Kimiyo ;
Rinaldo, Piero ;
Tortorelli, Silvia ;
Matern, Dietrich .
MOLECULAR GENETICS AND METABOLISM, 2019, 127 (03) :298-299
[27]   Laboratory monitoring of patients with hereditary tyrosinemia type I [J].
Schultz, Matthew J. ;
Netzel, Brian C. ;
Singh, Rani H. ;
Pino, Gisele B. ;
Gavrilov, Dimitar K. ;
Oglesbee, Devin ;
Raymond, Kimiyo M. ;
Rinaldo, Piero ;
Tortorelli, Silvia ;
Smith, Wendy E. ;
Matern, Dietrich .
MOLECULAR GENETICS AND METABOLISM, 2020, 130 (04) :247-254
[28]   TYROSINEMIA TYPE I: THE MOROCCAN EXPERIENCE IN THE DIAGNOSIS AND MONITORING [J].
Dahri, S. ;
Talbaoui, H. ;
Meskini, T. ;
Erreimi, N. ;
Vianey-Saban, C. ;
Chabraoui, L. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 :S26-S26
[29]   Current strategies for the treatment of hereditary tyrosinemia type I [J].
Ashorn M. ;
Pitkänen S. ;
Salo M.K. ;
Heikinheimo M. .
Pediatric Drugs, 2006, 8 (1) :47-54
[30]   A CASE OF THE TYROSINEMIA TYPE I IN UKRAINE: EXPERIENCE AND OUTCOME [J].
Pichkur, N. O. ;
Olkhovych, N. V. ;
Gorovenko, N. G. ;
Zakharova, E. Yu. ;
Baydakova, G. V. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 :S81-S81