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Volumn 25, Issue 7-8, 2012, Pages 805-808
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Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation
a
c
EGE UNIVERSITY
(Turkey)
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Author keywords
Glucokinase; Maturity onset diabetes of the young (MODY); Neonatal diabetes mellitus; Sulphonylurea
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Indexed keywords
C PEPTIDE;
GLIBENCLAMIDE;
GLICLAZIDE;
GLUCOKINASE;
GLUCOSE;
HEMOGLOBIN A1C;
INSULIN;
INSULIN ASPART;
INSULIN GLARGINE;
ISOPHANE INSULIN;
KETONE;
ADULT;
AGE;
ARTERIAL GAS;
ARTICLE;
BLOOD GAS ANALYSIS;
CASE REPORT;
CELL FATE;
CHILD;
CLINICAL FEATURE;
DEHYDRATION;
DIAPER DERMATITIS;
DRUG DOSE INCREASE;
DRUG DOSE REDUCTION;
ENVIRONMENTAL FACTOR;
FACIAL NERVE PARALYSIS;
FEMALE;
FEVER;
FLUID THERAPY;
GENE MUTATION;
GENETIC ASSOCIATION;
GENETIC SCREENING;
GENETIC VARIABILITY;
GLUCOSE BLOOD LEVEL;
GLUCOSURIA;
HEMOGLOBIN BLOOD LEVEL;
HETEROZYGOTE;
HOMOZYGOSITY;
HUMAN;
HYPERGLYCEMIA;
HYPOGLOSSAL NERVE PALSY;
HYPOTENSION;
KETONURIA;
LABORATORY TEST;
LARYNGEAL NERVE;
MALE;
METABOLIC REGULATION;
NAUSEA AND VOMITING;
NEONATAL WEIGHT LOSS;
NERVE PARALYSIS;
NEWBORN DIABETES MELLITUS;
NEWBORN SEPSIS;
NON INSULIN DEPENDENT DIABETES MELLITUS;
ORAL GLUCOSE TOLERANCE TEST;
PANCREAS ISLET BETA CELL;
PHYSICAL EXAMINATION;
POLYDIPSIA;
POLYURIA;
PROTEIN BLOOD LEVEL;
SCHOOL CHILD;
SEQUENCE ANALYSIS;
TACHYCARDIA;
AGE FACTORS;
CHILD;
DELAYED DIAGNOSIS;
DIABETES MELLITUS, TYPE 2;
FAMILY RELATIONS;
FEMALE;
GLUCOKINASE;
HOMOZYGOTE;
HUMANS;
INDIVIDUALITY;
INFANT;
MALE;
MUTATION, MISSENSE;
YOUNG ADULT;
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EID: 84867774551
PISSN: 0334018X
EISSN: 21910251
Source Type: Journal
DOI: 10.1515/jpem-2012-0077 Document Type: Article |
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Times cited : (6)
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References (10)
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