Sengers RC - Search Results

1

[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?].

Sengers RC, Hamel BC, Otten BJ, van Gils JF, de Pagter AG. Sengers RC, et al. Tijdschr Kindergeneeskd. 1985 Feb;53(1):31-4. Tijdschr Kindergeneeskd. 1985. PMID: 4039476 Dutch.

2

Growth hormone (GH) secretion in children with Noonan syndrome: frequently abnormal without consequences for growth or response to GH treatment.

Noordam C, van der Burgt I, Sweep CG, Delemarre-van de Waal HA, Sengers RC, Otten BJ. Noordam C, et al. Among authors: sengers rc. Clin Endocrinol (Oxf). 2001 Jan;54(1):53-9. doi: 10.1046/j.1365-2265.2001.01188.x. Clin Endocrinol (Oxf). 2001. PMID: 11167926

3

Spinal muscular atrophy combined with congenital heart disease: a report of two cases.

Mulleners WM, van Ravenswaay CM, Gabreëls FJ, Hamel BC, van Oort A, Sengers RC. Mulleners WM, et al. Among authors: sengers rc. Neuropediatrics. 1996 Dec;27(6):333-4. doi: 10.1055/s-2007-973805. Neuropediatrics. 1996. PMID: 9050054 No abstract available.

4

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial.

Noordam C, Van der Burgt I, Sengers RC, Delemarre-van de Waal HA, Otten BJ. Noordam C, et al. Among authors: sengers rc. Acta Paediatr. 2001 Aug;90(8):889-94. Acta Paediatr. 2001. PMID: 11529537 Clinical Trial.

5

Oculocutaneous albinism associated with motor neuron disease.

Hamel BC, Sengers RC, Stadhouders AM, Jaspar HH, Ter Laak HJ, Trijbels JM, Gabreëls-Festen AW. Hamel BC, et al. Among authors: sengers rc. Helv Paediatr Acta. 1978 Feb;32(6):487-93. Helv Paediatr Acta. 1978. PMID: 632111

6

The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.

Loeffen J, Smeitink J, Triepels R, Smeets R, Schuelke M, Sengers R, Trijbels F, Hamel B, Mullaart R, van den Heuvel L. Loeffen J, et al. Am J Hum Genet. 1998 Dec;63(6):1598-608. doi: 10.1086/302154. Am J Hum Genet. 1998. PMID: 9837812 Free PMC article.

7

[A patient with persistent hyperlysinemia].

Sengers RC, Trijbels JM, Corstiaensen JB. Sengers RC, et al. Tijdschr Kindergeneeskd. 1983 Feb;51(1):24-6. Tijdschr Kindergeneeskd. 1983. PMID: 6407142 Dutch.

8

[Mitochondrial myopathies].

Sengers RC, Stadhouders AM, Trijbels JM. Sengers RC, et al. Tijdschr Kindergeneeskd. 1988 Jun;56(3):110-5. Tijdschr Kindergeneeskd. 1988. PMID: 2842888 Dutch.

9

[Congenital myopathies].

Sengers RC, Gabreëls FJ, Boon JM. Sengers RC, et al. Ned Tijdschr Geneeskd. 1988 Jun 4;132(23):1079-81. Ned Tijdschr Geneeskd. 1988. PMID: 3386770 Dutch. No abstract available.

10

Preterm birth in Sjögren-Larsson syndrome.

Willemsen MA, Rotteveel JJ, van Domburg PH, Gabreëls FJ, Mayatepek E, Sengers RC. Willemsen MA, et al. Among authors: sengers rc. Neuropediatrics. 1999 Dec;30(6):325-7. doi: 10.1055/s-2007-973513. Neuropediatrics. 1999. PMID: 10706028

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