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Partial lipodystrophy in patients who have undergone hematopoietic stem cell transplantation during childhood: an institutional cross-sectional survey.The ratio of serum free triiodothyronine to free thyroxine in children: a retrospective database survey of healthy short individuals and patients with severe thyroid hypoplasia or central hypothyroidism.Abnormal adipose tissue distribution with unfavorable metabolic profile in five children following hematopoietic stem cell transplantation: a new etiology for acquired partial lipodystrophy.Ectopic calcification as discernible manifestation in neonates with pseudohypoparathyroidism type 1a.Prevalence of obesity, hyperlipemia and insulin resistance in children with suprasellar brain tumors.Classic Bartter syndrome complicated with profound growth hormone deficiency: a case report.Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism.Unfavorable lipoprotein profile in childhood cancer survivors with suprasellar brain tumors--a high Apo B level and increased small dense LDL-cholesterol.A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation.Compound heterozygous mutations in the gamma subunit gene of ENaC (1627delG and 1570-1G-->A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1.A male patient presenting with major clinical symptoms of glucocorticoid deficiency and skeletal dysplasia, showing a steroid pattern compatible with 17alpha-hydroxylase/17,20-lyase deficiency, but without obvious CYP17 gene mutations.Assessment of user-friendliness of the Norditropin FlexPro for pediatric patients treated with recombinant human growth hormone: results of an open-label user survey.Unnoticed maternal Graves' disease revealed by the baby's low free thyroxine in newborn screening: an underestimated condition supporting thyroid disease screening among pregnant women.Novel compound heterozygous mutations of the growth hormone-releasing hormone receptor gene in a case of isolated growth hormone deficiency.Analysis of mutations via protein expression studies in glycogen storage disease type IV: A report on a non-progressive form with a literature reviewNovel SLC12A1 (NKCC2) mutations in two families with Bartter syndrome type 1Growth hormone response to GH-releasing peptide-2 in childrenOverall usefulness of newborn screening for congenital hypothyroidism by using free thyroxine measurementSevere in utero under-virilization in a 46,XY patient with Silver-Russell syndrome with 11p15 loss of methylationDietary potassium restriction attenuates urinary sodium wasting in the generalized form of pseudohypoaldosteronism type 1Hyponatremia secondary to severe atopic dermatitis in early infancyCorrection to: Dietary potassium restriction attenuates urinary sodium wasting in the generalized form of pseudohypoaldosteronism type 1
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Q33594434-5F6FF3C4-AC8F-418A-9A6B-57C9D2CA6BB8Q35830724-9F4FC985-7931-483A-A904-758B2CFD3ED5Q37259059-04CA16F3-230A-48C8-A8C6-5E278CBF240CQ37423173-8358FA69-7FEC-4AAE-8FA1-C0FEC7D77DDAQ37732807-620E2220-BB40-4165-B48C-14408AA7EABEQ38174651-98BC4B5C-698E-46A3-B511-D90B3AA80E2BQ38468548-B0C2122C-18BE-4106-A0A6-8A3F29DFA1EEQ38473935-5EE33BD7-C72D-42B2-9891-A2F70B8CC480Q38485133-EDFC8043-CF3A-4703-9774-4F2C2F73DE6FQ38492042-F0652CFB-8656-4DB9-A2DA-70CC5A8335E9Q40822818-76C731BE-FDD0-41C7-8745-FB74E7FA769EQ43504716-3A96C36E-2D50-4877-B38F-11530964DD80Q48029405-F2ED6BE4-85AF-4750-B50A-1E5A21DAA6CFQ48378502-50EF5728-2EA2-44B3-BBF6-AB035379142CQ51058467-96BEE528-926C-490C-B58B-A3A35072663AQ58743384-4E2F413C-B075-4CE8-9C26-BD1AB1F21669Q81590889-81FB3E3C-7B85-4825-B3C2-F4B5DC77F851Q84597801-7E27040D-F0EB-4056-8A3C-E6E3506822C1Q87493782-A8EEE506-06DD-46EC-B61A-B0E9E2238BDBQ91196634-B3897A09-FCB9-4176-B87C-ECBE12ACCD6DQ92409581-4A49723B-8FDF-4D28-884B-4F4E72FC8C61Q93092158-8541309D-15CA-4029-8D06-6AB4AC759AF5Q94462588-7543D1CF-FF4A-41F5-AF74-5AD5580A263D
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Masanori Adachi
@ast
Masanori Adachi
@en
Masanori Adachi
@es
Masanori Adachi
@nl
Masanori Adachi
@sl
type
label
Masanori Adachi
@ast
Masanori Adachi
@en
Masanori Adachi
@es
Masanori Adachi
@nl
Masanori Adachi
@sl
prefLabel
Masanori Adachi
@ast
Masanori Adachi
@en
Masanori Adachi
@es
Masanori Adachi
@nl
Masanori Adachi
@sl
P106
P21
P31
P496
0000-0003-4747-3983
P569
2000-01-01T00:00:00Z