Page last updated: 2024-08-17

lysine and Bone Marrow Diseases

lysine has been researched along with Bone Marrow Diseases in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (66.67)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abukawa, D; Endoh, M; Hama, A; Hayasaka, K; Igarashi, Y; Ito, E; Kanai, M; Kanno, M; Kawakami, T; Mitsui, T; Noro, M; Sendo, D; Shirahata, E; Tono, C; Tsuchiya, S	1
Andria, G; Incerti, B; Parenti, G; Pecoraro, C; Sebastio, G; Strisciuglio, P; Terracciano, L	1
Borrone, C; Caruso, U; DiRocco, M; Garibotto, G; Picco, P; Rossi, GA; Taccone, A	1

Reviews

1 review(s) available for lysine and Bone Marrow Diseases

Article	Year
Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course. The Journal of pediatrics, 1995, Volume: 126, Issue:2 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Biopsy; Bone Marrow; Bone Marrow Diseases; Child; Child, Preschool; Female; Humans; Infant; Italy; Kidney; Lung; Lysine; Male; Retrospective Studies	1995

Other Studies

2 other study(ies) available for lysine and Bone Marrow Diseases

Article	Year
Genetic analysis of Shwachman-Diamond syndrome: phenotypic heterogeneity in patients carrying identical SBDS mutations. The Tohoku journal of experimental medicine, 2005, Volume: 206, Issue:3 Topics: Base Sequence; Bone and Bones; Bone Marrow Diseases; Child; Child, Preschool; Chromosomes; DNA; DNA Mutational Analysis; DNA Primers; Exocrine Pancreatic Insufficiency; Exons; Female; Frameshift Mutation; Gene Deletion; Genetic Variation; Heterozygote; Humans; Infant; Infant, Newborn; Introns; Japan; Karyotyping; Lysine; Male; Molecular Sequence Data; Mutation; Oligonucleotides; Osteochondrodysplasias; Phenotype; Polymerase Chain Reaction; Proteins; RNA, Messenger; Syndrome	2005
Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intolerance. European journal of pediatrics, 1993, Volume: 152, Issue:5 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anemia, Hemolytic; Bone Marrow Diseases; Child, Preschool; Humans; Infant; Kidney Diseases; Lysine; Male; Prognosis; Pulmonary Fibrosis; Time Factors	1993

Article

Year

Genetic analysis of Shwachman-Diamond syndrome: phenotypic heterogeneity in patients carrying identical SBDS mutations.

The Tohoku journal of experimental medicine, 2005, Volume: 206, Issue:3

Topics: Base Sequence; Bone and Bones; Bone Marrow Diseases; Child; Child, Preschool; Chromosomes; DNA; DNA Mutational Analysis; DNA Primers; Exocrine Pancreatic Insufficiency; Exons; Female; Frameshift Mutation; Gene Deletion; Genetic Variation; Heterozygote; Humans; Infant; Infant, Newborn; Introns; Japan; Karyotyping; Lysine; Male; Molecular Sequence Data; Mutation; Oligonucleotides; Osteochondrodysplasias; Phenotype; Polymerase Chain Reaction; Proteins; RNA, Messenger; Syndrome

2005

Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intolerance.

European journal of pediatrics, 1993, Volume: 152, Issue:5

Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anemia, Hemolytic; Bone Marrow Diseases; Child, Preschool; Humans; Infant; Kidney Diseases; Lysine; Male; Prognosis; Pulmonary Fibrosis; Time Factors

1993