"infantile sandhof disease" trang 5 - tải miễn phí từ tailieunhanh
Low birth weight contributed to increased serum IL-6 levels in infantile respiratory syncytial virus infection

Low birth weight contributed to increased serum IL-6 levels in infantile respiratory syncytial virus infection
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Isolated enophthalmos: An uncommon gateway to orbital tumors in pediatrics: 9 month-old female presenting with isolated enophthalmos as the unique sign of a metastatic orbital tumor: A case report

Isolated enophthalmos: An uncommon gateway to orbital tumors in pediatrics: 9 month-old female presenting with isolated enophthalmos as the unique sign of a metastatic orbital tumor: A case report
3    81    0
Development and validation of bile acid profile-based scoring system for identification of biliary atresia: A prospective study

Development and validation of bile acid profile-based scoring system for identification of biliary atresia: A prospective study
9    91    0
Combination of gamma-glutamyl transferase and liver stiffness measurement for biliary atresia screening at different ages: A retrospective analysis of 282 infants

Combination of gamma-glutamyl transferase and liver stiffness measurement for biliary atresia screening at different ages: A retrospective analysis of 282 infants
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Serial casting in early onset scoliosis: Syndromic scoliosis is no contraindication

Serial casting in early onset scoliosis: Syndromic scoliosis is no contraindication
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Hip joint pain in children with cerebral palsy and developmental dysplasia of the hip: Why are the differences so huge

Hip joint pain in children with cerebral palsy and developmental dysplasia of the hip: Why are the differences so huge
6    35    2
Canine infantile left ventricular noncompaction

Canine infantile left ventricular noncompaction
6    16    1
Rationale and design of ON-TRK: A novel prospective non-interventional study in patients with TRK fusion cancer treated with larotrectinib

Rationale and design of ON-TRK: A novel prospective non-interventional study in patients with TRK fusion cancer treated with larotrectinib
11    22    1
Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome

Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
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An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: A case report

An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: A case report
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