A. Kiss

发表

Inv dup del(4)(:p13 → p16.3::p16.3 → qter) in a girl without typical manifestations of Wolf–Hirschhorn syndrome

M. Riegel, P. Cotter, R. Rosa, 2009, American journal of medical genetics. Part A.

CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.

E. Bertini, R. Hennekam, H. Kayserili, 2007, American journal of human genetics.

Peduncular hallucinosis after sacrifice of veins of the petrosal venous complex for trigeminal neuralgia

A. Koerbel, A. Kiss, S. A. Wolf, 2007, Acta Neurochirurgica.

Poland syndrome associated with an aberrant subclavian artery and vascular abnormalities of the retina in a child exposed to misoprostol during pregnancy.

R. Rosa, G. Paskulin, P. Zen, 2007, Birth defects research. Part A, Clinical and molecular teratology.

Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

A. Janecke, M. Bros, C. Hübner, 2011, Nature Genetics.

[Chromosomal abnormalities in couples with history of recurrent abortion].

R. Rosa, G. Paskulin, P. Zen, 2009, Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia.

Combined transconjunctival-eyebrow approach providing minimally invasive access to all orbital quadrants. Technical note.

A. Koerbel, A. Kiss, V. R. Ferreira, 2007, Neurosurgical focus.

Salmonella thyroiditis: a case report and review of the literature.

T. Luvhengo, A. Kiss, A. Maraj, 2013, South African journal of surgery. Suid-Afrikaanse tydskrif vir chirurgie.

Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18.

G. Paskulin, A. Kiss, A. Carvalho, 2011, Anais brasileiros de dermatologia.

A patient presenting a 22q13 deletion associated with an apparently balanced translocation t(16;22): An illustrative case in the investigation of patients with low ARSA activity

M. Saraiva-Pereira, I. Schwartz, M. Riegel, 2012, Genetics and molecular biology.

Cardiac Surgery Unmasks Latent Hypoparathyroidism in a Child with the 22q11.2 Deletion Syndrome

Julio Cesar Sampaio P. Leite, A. Kiss, J. Huber, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Intraoperative diagnosis of pseudotumoral cerebellar neuroschistosomiasis

M. J. Serapião, A. Kiss, H. Appel, 2009 .

A Brazilian galactosialidosis patient given renal transplantation: A case report

R. Giugliani, I. Schwartz, A. d’Azzo, 2008, Journal of Inherited Metabolic Disease.

Pseudotumor of temporomandibular joint: destructive calcium pyrophosphate dihydrate arthropathy.

A. Kiss, Houpt Jb, Pritzker Kp, 1976, The Journal of rheumatology.