315 results on '"Hernández‐Martín, Angela"'
Search Results
2. Cardiocutaneous Desmosomal Disorders
3. Mucocutaneous manifestations in children hospitalized with COVID-19
4. Malnutrition in children with ichthyosis: Recommendations for monitoring from a multidisciplinary clinic experience
5. Clinical Features of NF1 in the Skin
6. Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome
7. Lesiones purpúricas en la infancia
8. Spanish consensus on infantile haemangioma
9. Consenso español sobre el hemangioma infantil
10. Cutaneous Mastocytosis With Predominant Infiltration of Promastocytes
11. Atrophic macules containing mesenchymal cells are precursor lesions of osteoma cutis in Albright hereditary osteodystrophy
12. 63 - Other Genodermatoses
13. Hereditary mucoepithelial dysplasia: A report of two patients
14. Cutaneous Drug Reactions in the Pediatric Population
15. Hyperpigmented macules on the face of young children: A series of 25 cases
16. A systematic review of clinical trials of treatments for the congenital ichthyoses, excluding ichthyosis vulgaris
17. Eosinophilic pustular folliculitis of infancy: A series of 15 cases and review of the literature
18. A Case with Juvenile Xanthogranuloma and Progressive Nodular Histiocytosis Overlap
19. Usefulness of Ultrasonography in the Diagnosis of Neonatal Dacryocystocele
20. Otorhinolaryngologic anomalies in children and young adults with congenital ichthyoses and keratinization disorders: Prospective assessment in a multidisciplinary clinic
21. Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in Spain
22. Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin
23. Papular epidermal nevus with “skyline” basal cell layer (PENS)
24. Two Cases of Autosomal Recessive Congenital Ichthyosis due to CYP4F22 Mutations: Expanding the Genotype of Self-Healing Collodion Baby
25. Clinical and Sonographic Classification of Neurofibromas in Children with Neurofibromatosis Type 1 – A Cluster Analysis.
26. Segmental pigmented purpuric dermatoses associated with other cutaneous segmental disorders: a retrospective case series
27. Clinical and Sonographic Classification of Neurofibromas in Children with Neurofibromatosis Type 1 – A Cluster Analysis
28. Scabies in a 14‐year‐old girl with superficial epidermolytic ichthyosis
29. Conradi‐Hünermann‐Happle syndrome with minimal signs
30. Hypopigmented macules in neurofibromatosis type 1: A case control study
31. Aplasia Cutis Congenita Associated with Fetus Papyraceus
32. Extensive Intracranial Arteriovenous Malformation in a Child with Aplasia Cutis Congenita
33. Nevus Anemicus: A Distinctive Cutaneous Finding in Neurofibromatosis Type 1
34. Congenital Erythematous Plaques and Papules on the Right Arm
35. A congenital folliculosebaceous cystic hamartoma on the nipple and areola.
36. Congenital Ulcer of the Buttock
37. Segmental Prurigo Pigmentosa
38. Nevus of Striated Muscle: A New Clinicopathologic Entity
39. Asymptomatic Skin-Colored Plaque in an 8-Year-Old Girl
40. Severe Demodex folliculorum–Associated Oculocutaneous Rosacea in a Girl Successfully Treated With Ivermectin
41. Contributors
42. Infantile transient smooth muscle contraction of the skin
43. Papular Epidermal Nevus with “Skyline” Basal Cell Layer (PENS) with Extracutaneous Findings
44. Neonatal Lupus Erythematosus Mimicking Extensive Capillary Malformation
45. Invasive Lymphatic Malformation (Gorham-Stout) of the Pelvis with Prominent Skin Involvement
46. Coste por proceso en el tratamiento quirúrgico del cáncer de piel
47. Cutaneous aspergillosis mimicking pancreatic and gouty panniculitis
48. Hereditary Mucoepithelial Dysplasia: Report of Two Sporadic Cases
49. Folliculocystic and collagen hamartoma of tuberous sclerosis complex
50. Aplasia Cutis Congenita and Other Anomalies Associated with Methimazole Exposure During Pregnancy
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