![Loading...](https://link.springer.com/static/c4a417b97a76cc2980e3c25e2271af3129e08bbe/images/pdf-preview/spacer.gif)
-
Article
Risk stratification for congenital diaphragmatic hernia by factors within 24 h after birth
To establish a simple risk stratification system for patients with congenital diaphragmatic hernia (CDH) based on postnatal information within 24 h after birth.
-
Article
Excess treatment reduction including anthracyclines results in higher incidence of relapse in core binding factor acute myeloid leukemia in children
-
Article
Prediction of postnatal outcomes in congenital diaphragmatic hernia using MRI signal intensity of the fetal lung
Prognostic prediction in prenatally diagnosed congenital diaphragmatic hernia (CDH) is needed. The aim of the study was to evaluate magnetic resonance imaging (MRI) signal intensity of the fetal lung as a pred...
-
Article
Voriconazole for both successful treatment of disseminated Trichosporon asahii infection and subsequent cord blood transplantation in an infant with acute myelogenous leukemia
-
Article
A case of thyrotropin-producing pituitary adenoma, accompanied by an increase in anti-thyrotropin receptor antibody after tumor resection
We describe a rare, but interesting, case of TSH-producing adenoma (TSHoma), accompanied by increases in both anti-TSH receptor antibody (TRAb) and thyroid-stimulating antibody (TSAb) after tumor resection. A ...
-
Article
Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen
-
Article
Gene analysis of the calcium channel 1 subunit and clinical studies for two patients with hypokalemic periodic paralysis
Hypokalemic periodic paralysis (HypoPP) is a skeletal muscle disorder in which episodic attacks of muscle weakness occur; they are associated with decreased serum potassium (K+) levels. Recent molecular approache...
-
Article
Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome
Mutations of the GATA1 gene on chromosome X have been found in almost all cases of transient myeloproliferative disorder and acute megakaryoblastic leukemia (AMKL) accompanying Down syndrome (DS). Although most G...
-
Article
Diagnosis of a case of Gitelman’s syndrome based on renal clearance studies and gene analysis of a novel mutation of the thiazide-sensitive Na-Cl cotransporter
Gitelman’s syndrome is a recessively inherited renal tubular disorder characterized by low plasma potassium and magnesium levels, reduced calcium excretion, metabolic alkalosis, and increased plasma renin acti...
-
Article
JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia
-
Article
Lack of clinical utility of minimal residual disease detection in allogeneic stem cell recipients with childhood acute lymphoblastic leukemia: multi-institutional collaborative study in Japan
The clinical utility of minimal residual disease (MRD) measurements following allogeneic stem cell transplantation (SCT) in childhood ALL is controversial. We therefore performed a multi-institutional study of...
-
Article
Intralobar bronchopulmonary sequestration evaluated by contrast-enhanced three-dimensional MR angiography
Bronchopulmonary sequestration (PS) is characterized by non-functioning lung tissue fed from one or several aberrant systemic arteries. The condition is diagnosed by visualizing the feeding arteries using non...
-
Article
Dipole bands in 142Gd
The high spin states of 142Gd were studied via the 111Cd(35Cl, 1p3n) reaction at 170 MeV. Three dipole cascades were found, one of which decayed to both the proton high-j particle states and the neutron high-j ho...
-
Article
Two-stage nuclear demagnetization refrigerator
Two-stage nuclear demagnetization has been performed using PrCu6 and Cu as coolants. The Cu nuclear stage reached temperatures as low as 10 ΜK with a rate of temperature rise of less than a few ΜK/h. The correspo...