Makimura M - Search Results

1

The signal transducer and activator of transcription 5B gene polymorphism contributes to the cholesterol metabolism in Japanese children with growth hormone deficiency.

Makimura M, Ihara K, Kojima-Ishii K, Nozaki T, Ohkubo K, Kohno H, Kishimoto J, Hara T. Makimura M, et al. Clin Endocrinol (Oxf). 2011 May;74(5):611-7. doi: 10.1111/j.1365-2265.2011.03980.x. Clin Endocrinol (Oxf). 2011. PMID: 21470284

2

Biotin deficiency in a glycogen storage disease type 1b girl fed only with glycogen storage disease-related formula.

Ihara K, Abe K, Hayakawa K, Makimura M, Kojima-Ishii K, Hara T. Ihara K, et al. Among authors: makimura m. Pediatr Dermatol. 2011 May-Jun;28(3):339-41. doi: 10.1111/j.1525-1470.2011.01238.x. Epub 2011 Mar 3. Pediatr Dermatol. 2011. PMID: 21371115

3

A girl with Hajdu-Cheney syndrome and premature ovarian failure.

Nozaki T, Ihara K, Makimura M, Kinjo T, Hara T. Nozaki T, et al. Among authors: makimura m. J Pediatr Endocrinol Metab. 2012;25(1-2):171-3. doi: 10.1515/jpem-2011-0443. J Pediatr Endocrinol Metab. 2012. PMID: 22570971

4

Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome.

Narazaki R, Makimura M, Sanefuji M, Fukamachi S, Akiyoshi H, So H, Yamamura K, Doisaki S, Kojima S, Ihara K, Hara T, Ohga S. Narazaki R, et al. Among authors: makimura m. Brain Dev. 2013 Aug;35(7):690-3. doi: 10.1016/j.braindev.2012.10.008. Epub 2012 Nov 8. Brain Dev. 2013. PMID: 23141186

5

Coagulopathy in patients with late-onset ornithine transcarbamylase deficiency in remission state: a previously unrecognized complication.

Ihara K, Yoshino M, Hoshina T, Harada N, Kojima-Ishii K, Makimura M, Hasegawa Y, Watanabe Y, Yamaguchi S, Hara T. Ihara K, et al. Among authors: makimura m. Pediatrics. 2013 Jan;131(1):e327-30. doi: 10.1542/peds.2012-0030. Epub 2012 Dec 3. Pediatrics. 2013. PMID: 23209112

6

Metabolic and immunological assessment of small-for-gestational-age children during one-year treatment with growth hormone: the clinical impact of apolipoproteins.

Kojima-Ishii K, Toda N, Okubo K, Tocan V, Ohyama N, Makimura M, Matsuo T, Ochiai M, Ohga S, Ihara K. Kojima-Ishii K, et al. Among authors: makimura m. Endocr J. 2018 Apr 26;65(4):449-459. doi: 10.1507/endocrj.EJ17-0485. Epub 2018 Feb 20. Endocr J. 2018. PMID: 29459555 Free article.

7

Placental mesenchymal dysplasia and fetal hematologic disorder.

Koga H, Makimura M, Tanaka H, Sumioki H. Koga H, et al. Among authors: makimura m. J Pediatr Hematol Oncol. 2014 Aug;36(6):e389-91. doi: 10.1097/MPH.0b013e31829d4542. J Pediatr Hematol Oncol. 2014. PMID: 23799527

8

N-terminal pro-brain natriuretic peptide as a useful predictor of early surgery in neonates with congenital heart diseases: a prospective observational study.

Makimura M, Koga H. Makimura M, et al. Pediatr Cardiol. 2014 Jan;35(1):77-81. doi: 10.1007/s00246-013-0744-y. Epub 2013 Jul 4. Pediatr Cardiol. 2014. PMID: 23824377

9

Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome.

Tanaka W, Oyama N, Makimura M, Miyako K. Tanaka W, et al. Among authors: makimura m. Pediatr Int. 2023 Jan-Dec;65(1):e15709. doi: 10.1111/ped.15709. Pediatr Int. 2023. PMID: 37968902 No abstract available.

10

A case of congenital hyperinsulinism presenting with diabetes after long-term diazoxide therapy.

Furuzono M, Makimura M, Miyako K. Furuzono M, et al. Among authors: makimura m. Diabetol Int. 2024 Apr 16;15(3):600-604. doi: 10.1007/s13340-024-00720-x. eCollection 2024 Jul. Diabetol Int. 2024. PMID: 39101184

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

69 results

Search Page

Filters