Fujieda Kenji | Department of Pediatrics, Asahikawa Medical College

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著作論文

The Role of N-Terminal Pro-B-Type Natriuretic Peptide in the Diagnosis of Congestive Heart Failure in Children : – Correlation With the Heart Failure Score and Comparison With B-Type Natriuretic Peptide –
43 Common origin of the Q258X mutation in StAR gene responsible for congenital aderenal lipoid hyperplasia in Japanese
The Role of N-Terminal Pro-B-Type Natriuretic Peptide in the Diagnosis of Congestive Heart Failure in Children : Correlation With the Heart Failure Score and Comparison With B-Type Natriuretic Peptide
A Male Patient with Severe Growth Retardation, Immunodeficiency and Diabetes Mellitus : A New Syndrome?
Case Study of a 15-Year-old Boy with McCune-Albright Syndrome Combined with Pituitary Gigantism : Effect of Octreotide-long Acting Release (LAR) and Cabergoline Therapy
Four Japanese Patients with Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism Caused by DAX-1 Gene Mutations : Mutant DAX-1 Failed to Repress Steroidogenic Acute Regulatory Protein (StAR) and Luteinizing Hormone β-subunit Gene Promoter Activi
Novel SLC12A1 (NKCC2) Mutations in Two Families with Bartter Syndrome Type 1
A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica
A Case of Achondroplasia Associated with Cervicomedullary-Junction Compression
Two Novel Mutations of Thiazide-Sensitive Na-Cl Cotransporter (TSC) Gene in Two Sporadic Japanese Patients with Gitelman Syndrome
Turner Syndrome with Crohn Disease
Two mutations of the Gsα gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia
Evaluation of Bone Mineral Density in Patients with Turner Syndrome
A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversal
A Japanese Case with Frasier Syndrome Caused by the Splice Junction Mutation of WT1 Gene
Mutations of the CYP21 Gene in Nonclassical Steroid 21-Hydroxylase Deficiency in Japan
Prenatal Diagnosis of Steroid 21-Hydroxylase Deficiency by the Modified Polymerase Chain Reaction to Detect Splice Site Mutation in the CYP21 Gene
PREDOMINANCE OF THE MUTATION AT 1138 OF THE cDNA FOR THE FIBROBLAST GROWTH FACTOR RECEPTOR 3 IN JAPANESE PATIENTS WITH ACHONDROPLASIA
A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
Monozygotic Twins with Discordant Sexual Phenotypes due to Different Rations of Mosaicism of 47, X, idic(Y), idic(Y)/46, X, idic(Y)/45, X
Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men
Low-dose Growth Hormone Treatment (0.175mg/kg/week) for Short Stature in Patients with Turner Syndrome : Data from KIGS Japan
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis : unusual clinical associations and novel claudin16 mutation in an Egyptian family
Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
Height Responses in Complete ldiopathic Growth Hormone Deficient Children Less Than Three Years of Age during Growth Hormone Therapy
A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure
Growth-Promoting and Psychological Effects of High-Dose Growth Hormone Treatment in Children with Intrauterine Growth Retardation
Acute disseminated encephalomyelitis in an infant with incontinentia pigmenti
Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
21-Hydroxylase Deficiency Presenting as Massive Bilateral Adrenal Masses in the Seventh Decade of Life
Development of Central Precocious Puberty After Surgical Resection in a Boy with Craniopharyngioma : Case Report
Postnatal development of brainstem serotonin-containing neurons projecting to lumbar spinal cord in rats
Gene Amplification as a Common Cause of lnherted Thyroxine-Binding Globulin Excess: Analysis of One Familial and Two Sporadic Cases
Effect of neonatal hypoxia on the development of intraspinal serotonergic fibers in relation to spinal motoneurons
Actigraphic assessment of sleep disorders in children with chronic fatigue syndrome
Endocrine Functions in Children with Suprasellar Germinoma
Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism

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