Heidemann P - Search Results

1

Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation.

Hehr U, Gross C, Diebold U, Wahl D, Beudt U, Heidemann P, Hehr A, Mueller D. Hehr U, et al. Among authors: heidemann p. Eur J Pediatr. 2004 Jul;163(7):347-52. doi: 10.1007/s00431-004-1459-0. Epub 2004 Apr 24. Eur J Pediatr. 2004. PMID: 15107988

2

Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease.

Frenzel S, Apel TW, Heidemann PH, Zerres K, Neumann HP, Dörr HG. Frenzel S, et al. Among authors: heidemann ph. Eur J Pediatr. 2001 Jul;160(7):421-4. doi: 10.1007/s004310100758. Eur J Pediatr. 2001. PMID: 11475579

3

Noonan syndrome: growth and clinical manifestations in 144 cases.

Ranke MB, Heidemann P, Knupfer C, Enders H, Schmaltz AA, Bierich JR. Ranke MB, et al. Among authors: heidemann p. Eur J Pediatr. 1988 Dec;148(3):220-7. doi: 10.1007/BF00441408. Eur J Pediatr. 1988. PMID: 3215198

4

Functioning thoracic paraganglioma: association with Von Hippel-Lindau syndrome.

Bender BU, Altehöfer C, Januszewicz A, Gärtner R, Schmidt H, Hoffmann MM, Heidemann PH, Neumann HP. Bender BU, et al. Among authors: heidemann ph. J Clin Endocrinol Metab. 1997 Oct;82(10):3356-60. doi: 10.1210/jcem.82.10.4050. J Clin Endocrinol Metab. 1997. PMID: 9329368

5

Effect of different oestrogen doses on final height reduction in girls with constitutional tall stature.

Grüters A, Heidemann P, Schlüter H, Stubbe P, Weber B, Helge H. Grüters A, et al. Among authors: heidemann p. Eur J Pediatr. 1989 Oct;149(1):11-3. doi: 10.1007/BF02024324. Eur J Pediatr. 1989. PMID: 2606121 Clinical Trial.

6

Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey.

Raue F, Pichl J, Dörr HG, Schnabel D, Heidemann P, Hammersen G, Jaursch-Hancke C, Santen R, Schöfl C, Wabitsch M, Haag C, Schulze E, Frank-Raue K. Raue F, et al. Among authors: heidemann p. Clin Endocrinol (Oxf). 2011 Dec;75(6):760-5. doi: 10.1111/j.1365-2265.2011.04142.x. Clin Endocrinol (Oxf). 2011. PMID: 21645025

7

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.

Gambineri E, Perroni L, Passerini L, Bianchi L, Doglioni C, Meschi F, Bonfanti R, Sznajer Y, Tommasini A, Lawitschka A, Junker A, Dunstheimer D, Heidemann PH, Cazzola G, Cipolli M, Friedrich W, Janic D, Azzi N, Richmond E, Vignola S, Barabino A, Chiumello G, Azzari C, Roncarolo MG, Bacchetta R. Gambineri E, et al. J Allergy Clin Immunol. 2008 Dec;122(6):1105-1112.e1. doi: 10.1016/j.jaci.2008.09.027. Epub 2008 Oct 25. J Allergy Clin Immunol. 2008. PMID: 18951619

8

Clinical and functional characterization of a patient carrying a compound heterozygous pericentrin mutation and a heterozygous IGF1 receptor mutation.

Müller E, Dunstheimer D, Klammt J, Friebe D, Kiess W, Kratzsch J, Kruis T, Laue S, Pfäffle R, Wallborn T, Heidemann PH. Müller E, et al. PLoS One. 2012;7(5):e38220. doi: 10.1371/journal.pone.0038220. Epub 2012 May 31. PLoS One. 2012. PMID: 22693602 Free PMC article.

9

[Hypophyseal microprolactinoma as a cause of delayed puberty].

Heidemann PH, Stubbe P. Heidemann PH, et al. Monatsschr Kinderheilkd. 1989 Nov;137(11):743-6. Monatsschr Kinderheilkd. 1989. PMID: 2514354 German.

10

A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria.

Kohlschütter A, Behbehani A, Langenbeck U, Albani M, Heidemann P, Hoffmann G, Kleineke J, Lehnert W, Wendel U. Kohlschütter A, et al. Among authors: heidemann p. Eur J Pediatr. 1982 Feb;138(1):32-7. doi: 10.1007/BF00442325. Eur J Pediatr. 1982. PMID: 7075624

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