PubMed for id: 419681

Year	Number of Results
1976	2
1977	2
1983	1
1984	1
1989	1
1990	1
1993	2
1997	1
1998	1
2001	1
2002	1
2003	3
2004	1
2009	1
2011	2
2013	1
2014	2
2016	1
2017	3
2018	3
2019	3
2020	2
2021	4
2022	3
2024	0

1

Ring substituted analogues of 5-aminomethyl-10,11-dihydro-dibenzo[a,d]cycloheptene (AMDH): potential modes of binding to the 5-HT(2A) receptor.

Peddi S, Roth BL, Glennon RA, Westkaemper RB. Peddi S, et al. Bioorg Med Chem Lett. 2003 Aug 4;13(15):2565-8. doi: 10.1016/s0960-894x(03)00504-3. Bioorg Med Chem Lett. 2003. PMID: 12852967

2

Acromesomelic dwarfism: a new variation.

Ferraz FG, Maroteaux P, Sousa JP, Alves T, Dias I, Ferraz E, Marques M, Santos L. Ferraz FG, et al. J Pediatr Orthop B. 1997 Jan;6(1):27-32. doi: 10.1097/01202412-199701000-00007. J Pediatr Orthop B. 1997. PMID: 9039664

3

Acromesomelic dwarfism in a child with an interesting family history.

Borrelli P, Fasanelli S, Marini R. Borrelli P, et al. Pediatr Radiol. 1983;13(3):165-8. doi: 10.1007/BF01624409. Pediatr Radiol. 1983. PMID: 6866577

4

Acromesomelic dwarfism: description of a patient and comparison with previously reported cases.

Hunter AG, Thompson MW. Hunter AG, et al. Hum Genet. 1976 Sep 10;34(1):107-13. doi: 10.1007/BF00284447. Hum Genet. 1976. PMID: 964999

5

Acromesomelic dwarfism: manifestations in childhood.

Langer LO Jr, Beals RK, Solomon IL, Bard PA, Bard LA, Rissman EM, Rogers JG, Dorst JP, Hall JG, Sparkes RS, Franken EA Jr. Langer LO Jr, et al. Am J Med Genet. 1977;1(1):87-100. doi: 10.1002/ajmg.1320010110. Am J Med Genet. 1977. PMID: 610427

6

[Acromesomelic dwarfism (author's transl)A1].

Pfeiffer RA. Pfeiffer RA. Rofo. 1976 Aug;125(2):171-3. doi: 10.1055/s-0029-1230437. Rofo. 1976. PMID: 133965 German.

7

A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type.

Langer LO Jr, Cervenka J, Camargo M. Langer LO Jr, et al. Hum Genet. 1989 Mar;81(4):323-8. doi: 10.1007/BF00283684. Hum Genet. 1989. PMID: 2703235

8

A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter-Thompson type.

Ullah A, Umair M, Muhammad D, Bilal M, Lee K, Leal SM, Ahmad W. Ullah A, et al. Ann Hum Genet. 2018 May;82(3):129-134. doi: 10.1111/ahg.12233. Epub 2018 Jan 10. Ann Hum Genet. 2018. PMID: 29322508 Free PMC article.

9

Encapsulation of amine dehydrogenase in hybrid titania nanoparticles by polyethylenimine coating and templated biomineralization.

Ren H, Zhang Y, Su J, Lin P, Wang B, Fang B, Wang S. Ren H, et al. J Biotechnol. 2017 Jan 10;241:33-41. doi: 10.1016/j.jbiotec.2016.11.006. Epub 2016 Nov 9. J Biotechnol. 2017. PMID: 27838254

10

A novel chimeric amine dehydrogenase shows altered substrate specificity compared to its parent enzymes.

Bommarius BR, Schürmann M, Bommarius AS. Bommarius BR, et al. Chem Commun (Camb). 2014 Dec 11;50(95):14953-5. doi: 10.1039/c4cc06527a. Chem Commun (Camb). 2014. PMID: 25347124

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