Uteroplacental insufficiency decreases forkhead box protein O1A (foxO1a) hepatic levels in perinatal and postnatal IUGR rats.
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- 2013
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- Abstract
Works matching IS 16879848 AND DT 2013 AND VI 2013 AND IP Suppl 1
Results: 263
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Association between exon-3 polymorphism of the GH Receptor(GHR) gene with catch growth in children born small for gestational age.
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- 2013
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Effect of intrauterine bodily development and nutritional status on the later body-length development of children. The MDN system.
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- 2013
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4
The neuro-cardio-facial-cutaneous syndrome - unity in diversity.
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- 2013
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5
Blood spots screening for identification of Fragile X Syndrome among intellectual disability students in Flores Island, INDONESIA.
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- 2013
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6
An unusual presentation of girl with down syndrome: Van-Wyk Grumbach syndrome.
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- 2013
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Vitamin D serum levels and vitamin D receptor FokIpolymorphism on tuberculosis children in Palembang, Indonesia.
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- 2013
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8
Fluid and electrolyte imbalance related to intracranial abnormality.
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- 2013
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9
Sexual precocity with pituitary macroadenoma and bilateral multicystic ovaries - a case report.
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- 2013
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10
Relapse in pituitary adenoma after resection.
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- 2013
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11
Multiple pituitary hormone deficiency: beware of combined hormones deficiency.
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- 2013
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12
Clinical course and endocrinological characteristics of prolactinoma in children and adolescents.
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- 2013
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13
Hypothalamic hamartoma with pubertas precox and gelastic seizure in a boy (Case Report).
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- 2013
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14
Etiology and clinical profile of children and adolescents with disorders of sex development (DSD) presenting with ambiguous external genitalia.
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- 2013
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15
Genotype and phenotype of Vietnamese patients with androgen insensitivity syndrome.
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- 2013
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16
Characteristic of patients with disorders of sex development (DSD) in Cipto Mangunkusumo Hospital, Jakarta.
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- 2013
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17
Sex rearing in individuals with 46,XY disorders of sex development prior to diagnosis.
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- 2013
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18
Clinical presentations and molecular characterization of Indonesian children with 5 alpha-reductase deficiency.
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- 2013
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19
A 45 X male patient with 7Q distal deletion and rearragement with SRY gene translocation; a case report.
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- 2013
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20
A novel mutation in the SRY gene causing 46 XY complete gonadal dysgenesis in a Chinese patient.
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- 2013
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21
The incidence of cryptorchidism among boys in some provinces in Indonesia.
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- 2013
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22
Penile length of newborns and children in Surakarta, Indonesia.
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- 2013
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23
Diagnosis of 5ɑ-reductase 2 deficiency: is measurement of dihydrotestosterone essential?
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- 2013
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24
Etiologies of 46,XY disorders of sex development (DSD): a collaborative study in Hong Kong.
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- 2013
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25
Clinical, hormonal and chromosomal analysis of undervirilized male/46XY DSD - a 3years experience of national institute of child health.
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- 2013
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26
A new celll model of glutaric acidemia type I and the toxicity research.
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- 2013
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27
Long-term outcome of a child with hyperinsulinism- hyperammonaemia syndrome.
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- 2013
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28
First case report of short-chain acyl-CoA dehydrogenase deficiency in China.
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- 2013
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29
Detection of inborn error of metabolisms by urine organic acid GC-MS in Southern China.
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- 2013
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30
Molecular genetics and phenotype of 26 Vietnamese patients with congenital hyperinsulinism.
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- 2013
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31
A discordant of blood glucose analysed by Glucometer and the Central lab method in an infant with Galactosemia.
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- 2013
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32
21 hypoglycemia cases with hyperinsulinemia.
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33
Short term outcome of congenital hyperinsulinism: case series.
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- 2013
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34
Geneotype and phenotype in 20 patients with glycogen storage disease type Ia.
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- 2013
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35
A case of sitosterolaemia with stomatocyticanaemia and thrombocytopenia treated with Ezetimibe with good response.
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- 2013
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36
POSTER PRESENTATION Open Access The Effect of Cumulative Dose of Glucocorticoids on Bone in Children with Inflammatory Bowel Disease (3-year Follow- up study).
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- 2013
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37
Targeted suppression of glutaryl-CoA dehydrogenase by lentivirus-mediated SHRNA and excessive intake of lysine induce the apoptosis of rat striatal neurons.
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- 2013
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38
Waist to height ratio; a simple and valid index for metabolic syndrome in Korean adolescents.
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- 2013
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39
A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene - the Barakat syndrome.
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- 2013
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40
Effect of osteogenesis imperfecta on children and their families.
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- 2013
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41
A Chinese boy with episodic ataxia and low CSF glucose.
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- 2013
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42
Osteogenesis imperfecta in children: Indosesian experiences.
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- 2013
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43
Vitamin D profile in healthy children aged 7-12 years old in Indonesia.
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- 2013
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44
Non-transfusion dependent hemoglobin E/β thalassemia had high prevalence of vitamin D deficiency than more severe patients who received regular blood transfusion and iron chelation therapy.
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- 2013
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45
Six monthly intravenous zoledronic acid in childhood osteoporosis.
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- 2013
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46
Solitary parathyroid adenoma presenting with spine fracture in a paediatric patient.
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- 2013
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47
Challenges in managing osteogenesis imperfecta patients in H. Adam Malik hospital, North Sumatera, Indonesia.
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- 2013
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48
An atypical 7Q11.2-Q21.11 deletion in a Williams- Beuren syndome patient.
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- 2013
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49
Adequate vitamin D status and adiposity contribute to bone health in peripubertal nonobese children.
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- 2013
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50
Age and seasonal variation of serum vitamin D levels in healthy school children and adolescents.
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- 2013
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