Bode H - Search Results

1

A case of phace syndrome and acquired hypopituitarism?

Denzer F, Denzer C, Lennerz BS, Bode H, Wabitsch M. Denzer F, et al. Among authors: bode h. Int J Pediatr Endocrinol. 2012 Jun 30;2012(1):20. doi: 10.1186/1687-9856-2012-20. Int J Pediatr Endocrinol. 2012. PMID: 22747526 Free PMC article.

2

Methylphenidate in children with monogenic obesity due to LEPR or MC4R deficiency improves feeling of satiety and reduces BMI-SDS-A case series.

Brandt S, von Schnurbein J, Lennerz B, Kohlsdorf K, Vollbach H, Denzer C, Bode H, Hebebrand J, Wabitsch M. Brandt S, et al. Among authors: bode h. Pediatr Obes. 2020 Jan;15(1):e12577. doi: 10.1111/ijpo.12577. Epub 2019 Oct 31. Pediatr Obes. 2020. PMID: 31670905

3

[Clinical impact of fetal MRI in addition to ultrasonography in brain anomalies--three case reports].

Strunz K, Schmitz B, Boll D, Bode H, Terinde R. Strunz K, et al. Among authors: bode h. Ultraschall Med. 2007 Aug;28(4):416-20. doi: 10.1055/s-2007-963025. Epub 2007 Jun 28. Ultraschall Med. 2007. PMID: 17599280 German.

4

Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia - further expansion of the phenotypic spectrum.

Lühl S, Bode H, Schlötzer W, Bartsakoulia M, Horvath R, Abicht A, Stenzel M, Kirschner J, Grünert SC. Lühl S, et al. Among authors: bode h. Orphanet J Rare Dis. 2016 Oct 21;11(1):140. doi: 10.1186/s13023-016-0525-9. Orphanet J Rare Dis. 2016. PMID: 27769281 Free PMC article.

5

Calcifying arteriopathy in the basal ganglia in human immunodeficiency virus infection.

Bode H, Rudin C. Bode H, et al. Pediatr Radiol. 1995;25(1):72-3. doi: 10.1007/BF02020858. Pediatr Radiol. 1995. PMID: 7761176

6

Non calcific vasculopathy in the basal ganglia.

Bode H, Rudin C, Bubl R. Bode H, et al. Klin Padiatr. 1991 Sep-Oct;203(5):350-3. doi: 10.1055/s-2007-1025451. Klin Padiatr. 1991. PMID: 1658431

7

[Children of drug-dependent mothers--personal experiences and review of the literature].

Bode H, Fabian T, Rudin C, Nars PW, Heinzl S. Bode H, et al. Klin Padiatr. 1992 Mar-Apr;204(2):92-7. doi: 10.1055/s-2007-1025329. Klin Padiatr. 1992. PMID: 1583858 German.

8

Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease.

Cario H, Smith DE, Blom H, Blau N, Bode H, Holzmann K, Pannicke U, Hopfner KP, Rump EM, Ayric Z, Kohne E, Debatin KM, Smulders Y, Schwarz K. Cario H, et al. Among authors: bode h. Am J Hum Genet. 2011 Feb 11;88(2):226-31. doi: 10.1016/j.ajhg.2011.01.007. Am J Hum Genet. 2011. PMID: 21310277 Free PMC article.

9

Congenital null mutations of the FOLR1 gene: a progressive neurologic disease and its treatment.

Cario H, Bode H, Debatin KM, Opladen T, Schwarz K. Cario H, et al. Among authors: bode h. Neurology. 2009 Dec 15;73(24):2127-9. doi: 10.1212/WNL.0b013e3181c679df. Neurology. 2009. PMID: 20018644 No abstract available.

10

Age dependence of flow velocities in basal cerebral arteries.

Bode H, Wais U. Bode H, et al. Arch Dis Child. 1988 Jun;63(6):606-11. doi: 10.1136/adc.63.6.606. Arch Dis Child. 1988. PMID: 3389890 Free PMC article.

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