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    1. Cerebellar Changes in Guinea Pig Offspring Following Suppression of Neurosteroid Synthesis During Late Gestation The Cerebellum · 2016 · 9 citations
    2. Cerebellar Medulloblastoma: Treatment by Irradiation of the Whole Central Nervous System Acta Radiologica · 1953 · 1 citations
    3. Cerebellar Medulloblastoma: Treatment by Irradiation of the Whole Central Nervous System Acta radiologica · 1953 · 163 citations
    4. Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome” European journal of pediatrics · 2002 · 5 citations
    5. Abnormalities of Purkinje Cell Arborization in Brindled Mouse Cerebellum Journal of Neuropathology & Experimental Neurology · 1985 · 23 citations
    6. Adaptive Balance in Posterior Cerebellum Frontiers in Neurology · 2021 · 21 citations
    7. Mechanism of progesterone neuroprotection of rat cerebellar Purkinje cells following oxygen–glucose deprivation European Journal of Neuroscience · 2006 · 83 citations
    8. BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin Nature Genetics · 1999 · 117 citations
    9. Inhibition of neurosteroid synthesis increases asphyxia-induced brain injury in the late gestation fetal sheep Neuroscience · 2007 · 100 citations
    10. Effects of Subchronic Finasteride Treatment and Withdrawal on Neuroactive Steroid Levels and Their Receptors in the Male Rat Brain Neuroendocrinology · 2015 · 33 citations
    11. Exploring the Impact of the Microbiome on Neuroactive Steroid Levels in Germ-Free Animals International journal of molecular sciences · 2021 · 11 citations
    12. Thallium poisoning: emphasis on early diagnosis and response to haemodialysis Postgraduate Medical Journal · 2003 · 60 citations
    13. STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Orphanet Journal of Rare Diseases · 2014 · 65 citations
    14. Role of neurosteroids in regulating cell death and proliferation in the late gestation fetal brain Neuroscience · 2009 · 76 citations
    15. Panel Session Neuropsychopharmacology · 2004
    16. SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder Cell · 2010 · 260 citations
    17. An X-traordinary stroke The Lancet · 2011 · 5 citations
    18. Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita Science Advances · 2025 · 3 citations
    19. Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature Pediatric neurology · 2008 · 23 citations
    20. Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia British Journal of Dermatology · 2007 · 17 citations
    21. Rhombencephalosynapsis presenting antenatally with ventriculomegaly/hydrocephalus in a likely case of Gomez–López-Hernández syndrome Clinical dysmorphology · 2006 · 18 citations
    22. Numerical Methods for Decision-Making in Clinical Care: Where to Now? Journal of the Royal Society of Medicine · 1988
    23. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation Nature genetics · 2000 · 694 citations
    24. The Effect of Copper Supplementation on the Brindled Mouse Journal of Neuropathology & Experimental Neurology · 1981 · 40 citations
    25. Ethanol‐induced elevation of 3α‐hydroxy‐5α‐pregnan‐20‐one does not modulate motor incoordination in rats Alcoholism Clinical and Experimental Research · 2004 · 26 citations
    26. Abnormal Saccadic Oscillations Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Encephalopathy and Ataxia Movement Disorders Clinical Practice · 2020 · 11 citations
    27. Cleave but not leave: Astrotactin proteins in development and disease IUBMB life · 2017 · 8 citations
    28. Analysis of androgen receptor expression and activity in the mouse brain Scientific Reports · 2024
    29. Diagnosed with primary adrenal insufficiency? search adrenoleukodystrophy-two brothers presented with similar phenotype International Journal of Research in Medical Sciences · 2023
    30. Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument Neuropediatrics · 2004 · 80 citations