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Results 1 - 7 of 7 for rocha syndrome
  1. Sjögren syndrome 
    ... 3390/ijms21020650. Citation on PubMed de Paiva CS, Rocha EM. Sjogren syndrome: what and where are we looking for? Curr ...
    https://medlineplus.gov/genetics/condition/sjogren-syndrome - Genetics
  2. Heterotaxy syndrome 
    ... B, Thauvin C, Maltret A, Dauphin C, Goncalves-Rocha M, Teboul M, Blanchet P, Roume J, Gronier ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  3. Schinzel-Giedion syndrome 
    ... for Rare Disorders (NORD) SCHINZEL-GIEDION MIDFACE RETRACTION ... M, Nur BG, Mihci E, Moreira LM, Borges Ferreira V, Horovitz DD, da Rocha KM, Jezela-Stanek A, Brooks AS, Reutter H, ...
    https://medlineplus.gov/genetics/condition/schinzel-giedion-syndrome - Genetics
  4. Primary macronodular adrenal hyperplasia 
    ... Registry: Acth-independent macronodular adrenal hyperplasia 2 Cushing syndrome ... MY, Mariani BM, Almeida MQ, Tremblay J, Hamet P, Bourdeau I, Zerbini MC, Pereira MA, Gomes GC, Rocha Mde S, Chambo JL, Lacroix A, Mendonca BB, ...
    https://medlineplus.gov/.../primary-macronodular-adrenal-hyperplasia - Genetics
  5. Mitochondrial complex V deficiency 
    ... DEFICIENCY, NUCLEAR TYPE 3; MC5DN3 PubMed Alston CL, Rocha MC, Lax NZ, Turnbull DM, Taylor RW. The ... synthase assembly defect: further delineation of a new syndrome. J Med Genet. 2011 Mar;48(3):177- ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  6. Mitochondrial complex I deficiency 
    ... DEFICIENCY, NUCLEAR TYPE 1; MC1DN1 PubMed Alston CL, Rocha MC, Lax NZ, Turnbull DM, Taylor RW. The ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  7. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... on PubMed Lin J, Chiconelli Faria E, Da Rocha AJ, Rodrigues Masruha M, Pereira Vilanova LC, Scheper ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics