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Publications by Tomonobu Hasegawa

Gonadal Macrophage Infiltration in Congenital Lipoid Adrenal Hyperplasia

European Journal of Endocrinology

English

Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients With Congenital Hypopituitarism

PLoS ONE

Multidisciplinary

2012

English

Hypoglycemia Associated With L-Asparaginase in Acute Lymphoblastic Leukemia Treatment: A Case Report

Experimental Hematology and Oncology

English

A Novel KAL1 Mutation Is Associated With Combined Pituitary Hormone Deficiency

Human Genome Variation

English

A Neonatal Case of HDR Syndrome and a Vascular Ring With a Novel GATA3 Mutation

Human Genome Variation

English

Two Novel Mutations of the CYP11B2 Gene in a Japanese Patient With Aldosterone Deficiency Type 1

English

Unilateral Adrenalectomy Can Be an Alternative Therapy for Infantile Onset Cushing’ S Syndrome Caused by ACTHindependent Macronodular Adrenal Hyperplasia With McCune-Albright Syndrome

English

Responses to the Letter to the Editor “Does Growth-Hormone Treatment Affect Patients With and Without a Mitochondrial Disorder Differentially ?” (Vol. 27, No. 2, P. 107–108, 2018)

Clinical Pediatric Endocrinology

English

Effect of Growth Hormone Treatment on Quality of Life in Japanese Children With Growth Hormone Deficiency: An Analysis From a Prospective Observational Study

Clinical Pediatric Endocrinology

English

Association Between Graves^|^rsquo; Disease and Renal Coloboma Syndrome: A Case Report

Clinical Pediatric Endocrinology

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Tomonobu Hasegawa

Gonadal Macrophage Infiltration in Congenital Lipoid Adrenal Hyperplasia

Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients With Congenital Hypopituitarism

Hypoglycemia Associated With L-Asparaginase in Acute Lymphoblastic Leukemia Treatment: A Case Report

A Novel KAL1 Mutation Is Associated With Combined Pituitary Hormone Deficiency

A Neonatal Case of HDR Syndrome and a Vascular Ring With a Novel GATA3 Mutation

Two Novel Mutations of the CYP11B2 Gene in a Japanese Patient With Aldosterone Deficiency Type 1

Unilateral Adrenalectomy Can Be an Alternative Therapy for Infantile Onset Cushing’ S Syndrome Caused by ACTHindependent Macronodular Adrenal Hyperplasia With McCune-Albright Syndrome

Responses to the Letter to the Editor “Does Growth-Hormone Treatment Affect Patients With and Without a Mitochondrial Disorder Differentially ?” (Vol. 27, No. 2, P. 107–108, 2018)

Effect of Growth Hormone Treatment on Quality of Life in Japanese Children With Growth Hormone Deficiency: An Analysis From a Prospective Observational Study

Association Between Graves^|^rsquo; Disease and Renal Coloboma Syndrome: A Case Report