Found: 41
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Osteopontin expression in the liver with severe perisinusoidal fibrosis: Autopsy case of Down syndrome with transient myeloproliferative disorder.
- Published in:
- Pathology International, 2008, v. 58, n. 1, p. 64, doi. 10.1111/j.1440-1827.2007.02191.x
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- Publication type:
- Article
Assessment of a New Piezoelectric Transducer Sensor for Noninvasive Cardiorespiratory Monitoring of Newborn Infants in the NICU.
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- Neonatology (16617800), 2010, v. 98, n. 2, p. 179, doi. 10.1159/000283994
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- Publication type:
- Article
Lidocaine-dependent Early Infantile Status Epilepticus with Highly Suppressed EEG.
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- Epilepsia (Series 4), 2002, v. 43, n. 2, p. 201, doi. 10.1046/j.1528-1157.2002.25301.x
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- Publication type:
- Article
Identification and Characterization of Cellulose-Binding Domains in Xylanase A of Clostridium stercorarium.
- Published in:
- Annals of the New York Academy of Sciences, 1996, v. 782, n. 1, p. 241, doi. 10.1111/j.1749-6632.1996.tb40565.x
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- Publication type:
- Article
Acute cerebellitis.
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- Cerebellum, 2002, v. 1, n. 3, p. 223, doi. 10.1080/14734220260418457
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- Publication type:
- Article
Increased numbers of macrophages in tracheal aspirates in premature infants with funisitis.
- Published in:
- Pediatrics International, 2008, v. 50, n. 2, p. 184, doi. 10.1111/j.1442-200X.2008.02558.x
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- Publication type:
- Article
X-linked adrenal hypoplasia congenita: Testicular histology before puberty.
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- Pediatrics International, 2007, v. 49, n. 4, p. 526, doi. 10.1111/j.1442-200X.2007.02416.x
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- Publication type:
- Article
Novel mutation of methylmalonyl-CoA mutase gene causing the mut <sup>0</sup> form of methylmalonic acidemia in a Japanese girl.
- Published in:
- Pediatrics International, 2007, v. 49, n. 2, p. 232, doi. 10.1111/j.1442-200X.2007.02325.x
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- Publication type:
- Article
A molecular lesion in a Japanese patient with severe phenotype of 3-methylglutaconic aciduria type I.
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- Pediatrics International, 2005, v. 47, n. 6, p. 684, doi. 10.1111/j.1442-200x.2005.02130.x
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- Publication type:
- Article
Luteinizing hormone-releasing hormone analog treatment for a criminal sexual habit caused by male precocious puberty.
- Published in:
- 2005
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- Publication type:
- Letter
Patient Report Familial mediterranean fever medicated with an herbal medicine in Japan.
- Published in:
- Pediatrics International, 2004, v. 46, n. 1, p. 81, doi. 10.1111/j.1328-0867.2004.01831.x
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- Publication type:
- Article
Case of congenital infection with Candida glabrata in one infant in a set of twins.
- Published in:
- Pediatrics International, 2002, v. 44, n. 4, p. 449, doi. 10.1046/j.1442-200X.2002.01565.x
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- Publication type:
- Article
Ala/Thr60 variant of the Leydig insulin-like hormone is not associated with cryptorchidism in the Japanese population.
- Published in:
- Pediatrics International, 2001, v. 43, n. 3, p. 256, doi. 10.1046/j.1442-200X.2001.01390.x
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- Publication type:
- Article
Neonatal intrahepatic cholestasis with hepatic siderosis and steatosis.
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- Pediatrics International, 1998, v. 40, n. 2, p. 150, doi. 10.1111/j.1442-200X.1998.tb01901.x
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- Publication type:
- Article
Effect of weight changes on serum transaminase activities in obese children.
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- Pediatrics International, 1997, v. 39, n. 2, p. 210, doi. 10.1111/j.1442-200X.1997.tb03583.x
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- Publication type:
- Article
Relationship of feeding modality to clinical features in Japanese infants with idiopathic neonatal hepatitis of the non-familial form.
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- Pediatrics International, 1996, v. 38, n. 4, p. 328, doi. 10.1111/j.1442-200X.1996.tb03500.x
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- Publication type:
- Article
Relationships between clinical and histological profiles of non-familial idiopathic neonatal hepatitis.
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- Pediatrics International, 1996, v. 38, n. 3, p. 242, doi. 10.1111/j.1442-200X.1996.tb03478.x
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- Publication type:
- Article
The relationship between serum transaminase activities and fatty liver in children with simple obesity.
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- Pediatrics International, 1995, v. 37, n. 5, p. 621, doi. 10.1111/j.1442-200X.1995.tb03389.x
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- Publication type:
- Article
Application of nasal septal cartilage in a combined transorbital and transnasal approach for orbital wall reconstruction.
- Published in:
- Archives of Plastic Surgery, 2021, v. 48, n. 2, p. 217, doi. 10.5999/aps.2020.01312
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- Publication type:
- Article
Changes in patterns of left ventricular diastolic filling revealed by Doppler echocardiography in infants with ventricular septal defect.
- Published in:
- 1998
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- Publication type:
- journal article
Fatal neonatal hypertrophic cardiomyopathy with severe stenosis of the right ventricular outflow tract: echocardiographic diagnosis and potential therapy.
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- Cardiology in the Young, 1999, v. 9, n. 1, p. 63, doi. 10.1017/S104795110000740X
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- Publication type:
- Article
Chylous ascites associated with atrioventricular valve regurgitation after Blalock-Taussig shunt.
- Published in:
- 1996
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- Publication type:
- journal article
Changes in transmitral and pulmonary venous flow patterns in the first day of life.
- Published in:
- 1995
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- Publication type:
- journal article
Correlation Between Right Ventricular Tei Index by Tissue Doppler Imaging and Pulsed Doppler Imaging in Fetuses.
- Published in:
- Pediatric Cardiology, 2008, v. 29, n. 4, p. 739, doi. 10.1007/s00246-008-9215-2
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- Publication type:
- Article
Paradoxical Relationship Between B-type Natriuretic Peptide and Pulmonary Vascular Resistance in Patients with Ventricular Septal Defect and Concomitant Severe Pulmonary Hypertension.
- Published in:
- Pediatric Cardiology, 2008, v. 29, n. 1, p. 65, doi. 10.1007/s00246-007-9037-7
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- Publication type:
- Article
Johanson-Blizzard Syndrome: Loss of Glucagon Secretion Response to Insulin-induced Hypoglycemia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2004, v. 17, n. 8, p. 1141, doi. 10.1515/jpem.2004.17.8.1141
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- Publication type:
- Article
Significant Decrease in Tropoelastin Gene Expression in Fibroblasts from a Japanese Costello Syndrome Patient with Impaired Elastogenesis and Enhanced Proliferation.
- Published in:
- Journal of Biochemistry, 2006, v. 140, n. 2, p. 193, doi. 10.1093/jb/mvj146
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- Publication type:
- Article
Recurrent URAT1 gene mutations and prevalence of renal hypouricemia in Japanese.
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- Pediatric Nephrology, 2005, v. 20, n. 5, p. 576, doi. 10.1007/s00467-005-1830-z
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- Publication type:
- Article
Renovascular hypertension due to antithrombin deficiency in childhood.
- Published in:
- Pediatric Nephrology, 2004, v. 19, n. 11, p. 1294, doi. 10.1007/s00467-004-1592-z
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- Publication type:
- Article
Aseptic Meningitis Associated With Cephalosporins in an Infant With Trisomy 21.
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- Journal of Child Neurology, 2007, v. 22, n. 6, p. 780, doi. 10.1177/0883073807304016
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- Publication type:
- Article
Restricted usage of T-cell receptor α-chain variable region (TCRAV) and T-cell receptor β-chain variable region (TCRBV) repertoires after human allogeneic haematopoietic transplantation.
- Published in:
- British Journal of Haematology, 2000, v. 109, n. 4, p. 759, doi. 10.1046/j.1365-2141.2000.02080.x
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- Publication type:
- Article
Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 12, p. 2247, doi. 10.1093/hmg/8.12.2247
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- Publication type:
- Article
Acute cerebellitis caused by Coxiella burnetii.
- Published in:
- 1999
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- Publication type:
- journal article
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter.
- Published in:
- Nature Genetics, 1999, v. 21, n. 1, p. 91, doi. 10.1038/5030
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- Publication type:
- Article
Five novel SLC7A7 variants and y<sup>+</sup>L gene-expression pattern in cultured lymphoblasts from Japanese patients with lysinuric protein intolerance.
- Published in:
- Human Mutation, 2002, v. 20, n. 5, p. 375, doi. 10.1002/humu.10140
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- Publication type:
- Article
A cluster of lysinuric protein intolerance (LPI) patients in a northern part of Iwate, Japan due to a founder effect.
- Published in:
- Human Mutation, 2000, v. 16, n. 3, p. 270, doi. 10.1002/1098-1004(200009)16:3<270::AID-HUMU14>3.0.CO;2-J
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- Publication type:
- Article
SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families.
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- Human Mutation, 2000, v. 15, n. 4, p. 367, doi. 10.1002/(SICI)1098-1004(200004)15:4<367::AID-HUMU9>3.0.CO;2-C
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- Publication type:
- Article
Mutational analyses of AVPR2 gene in three Japanese families with X-linked nephrogenic diabetes insipidus: Two recurrent mutations, R137H and ΔV278, caused by the hypermutability at CpG dinucleotides.
- Published in:
- Human Mutation, 1998, v. 11, p. S278, doi. 10.1002/humu.1380110188
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- Publication type:
- Article
Identification of a missense mutation (S436R) in the acid sphingomyelinase gene from a Japanese patient with type B Niemann-Pick disease.
- Published in:
- Human Mutation, 1992, v. 1, n. 1, p. 70, doi. 10.1002/humu.1380010111
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- Publication type:
- Article
Prolonged activation of the hypothalamus– pituitary–gonadal axis in a child with X-linked adrenal hypoplasia congenita.
- Published in:
- Clinical Endocrinology, 2000, v. 53, n. 1, p. 127, doi. 10.1046/j.1365-2265.2000.01037.x
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- Publication type:
- Article
Mutation of the myelin Po gene in Charcot — Marie — Tooth neuropathy type 1B.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 9, p. 1369
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- Publication type:
- Article