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phosphorus and Chromosome Deletion

phosphorus has been researched along with Chromosome Deletion in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Denkboy Öngen, Y; Eren, E; Özemri Sağ, Ş; Temel, ŞG1
Bastepe, M; Jüppner, H; Linglart, A; Lteif, AN; Mahmud, FH1
Choi, JH; Kim, GH; Kim, Y; Park, IS; Seo, EJ; Shin, YL; Yoo, HW1
Baldini, A; Botta, A; Bradley, A; Carattini-Rivera, S; Cheah, YC; Jurecic, V; Lindsay, EA; Rosenblatt, HM1
De La Villemarque, R; Derrien, C; Henry, C; Maugendre, D; Odent, S; Poirier, JY1
Ausenda, C; Barbiroli, B; Bresolin, N; Comi, GP; Gallanti, A; Lugaresi, E; Martinelli, P; Montagna, P; Scarlato, G; Zaniol, P1

Other Studies

6 other study(ies) available for phosphorus and Chromosome Deletion

ArticleYear
An Endocrinological Perspective on 22q11.2 Deletion Syndrome: A Single-center Experience
    Journal of clinical research in pediatric endocrinology, 2023, 08-23, Volume: 15, Issue:3

    Topics: Calcium; Chromosome Deletion; Diabetes Mellitus, Type 2; DiGeorge Syndrome; Dwarfism; Humans; Hypocalcemia; Hypoparathyroidism; In Situ Hybridization, Fluorescence; Parathyroid Hormone; Phosphorus

2023
Molecular diagnosis of pseudohypoparathyroidism type Ib in a family with presumed paroxysmal dyskinesia.
    Pediatrics, 2005, Volume: 115, Issue:2

    Topics: Child; Chorea; Chromosome Deletion; Diagnostic Errors; Female; Humans; Hypocalcemia; Pedigree; Phosphorus; Pseudohypoparathyroidism

2005
Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.
    Hormone research, 2005, Volume: 63, Issue:6

    Topics: Body Height; Calcium; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 22; Endocrine System Diseases; Female; Humans; Hypocalcemia; Hypoparathyroidism; Infant; Infant, Newborn; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Longitudinal Studies; Male; Parathyroid Hormone; Phosphorus; Thyroid Diseases

2005
Congenital heart disease in mice deficient for the DiGeorge syndrome region.
    Nature, 1999, Sep-23, Volume: 401, Issue:6751

    Topics: Adaptor Proteins, Vesicular Transport; Animals; Aorta, Thoracic; Calcium; Chromosome Deletion; DiGeorge Syndrome; Disease Models, Animal; Female; Genetic Complementation Test; Genetic Engineering; Heart Defects, Congenital; Intercellular Signaling Peptides and Proteins; Intracellular Signaling Peptides and Proteins; Lymphocyte Count; Male; Mice; Mice, Inbred C57BL; Parathyroid Hormone; Phosphorus; Proteins

1999
[Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation].
    Annales d'endocrinologie, 2001, Volume: 62, Issue:6

    Topics: Abnormalities, Multiple; Adult; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 22; Diagnosis, Differential; Face; Female; Fibrous Dysplasia, Polyostotic; Humans; Hypercalcemia; Hypoparathyroidism; In Situ Hybridization, Fluorescence; Infant, Newborn; Intellectual Disability; Obesity; Parathyroid Hormone; Phenotype; Phosphorus; Pregnancy; Pregnancy Complications; Pseudohypoparathyroidism; Purpura, Thrombocytopenic, Idiopathic; Scoliosis; Syndrome; Velopharyngeal Insufficiency

2001
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.
    Journal of the neurological sciences, 1991, Volume: 104, Issue:2

    Topics: Adult; Blotting, Southern; Brain; Chromosome Deletion; DNA Restriction Enzymes; DNA, Mitochondrial; Electron Transport Complex IV; Energy Metabolism; Female; Histocytochemistry; Humans; Magnetic Resonance Spectroscopy; Migraine Disorders; Mitochondria, Muscle; Muscles; Oligodeoxyribonucleotides; Phosphorus; RNA, Ribosomal; RNA, Transfer; RNA, Transfer, Leu

1991